IQVIA

Job OverviewProvide comprehensive clinical lab data expertise as part of a team to develop and maintain Laboratory Data Management (LDM) tasks for the studies awarded to Q squared solutions and meets the external client data reporting needs. May be required to support the development of new systems and processes related to the electronic data transfer process, or the configuration of business rules and master data in study and laboratory information systems.  Understand and comply with core standard operating procedures and working instructions. Essential Functions Capable of taking up, independently or providing inputs for, SAS programming activities pertaining to ongoing study requirements or any other adhoc projects in the department Create and/or review all appropriate data management documents Understand and comply with core standard operating procedures and working instructions Develop and maintain good communications and working relationships with LDM team. Serve as back-up for other Data Team Leads Interact with internal and external team members to negotiate timelines and responsibilities Train and mentor junior staff in DM expertise Ensure service and quality meet agreed upon timelines and deliverables in data transmission agreements. Ensure quality checks performed on data files before transmission and obtain peer-review where required. Review own work for accuracy and completeness Record all evidence of the data transmission process from data file definition to closure of study Ensure that all specification and design documentation are filed and stored according to company policy Ensure the internal and external customer queries are timely addressed and resolved effectively Multiple communication styles and skill to effectively broker, audience specific [peers, senior team members, internal/external customers] business and interpersonal relationships that lead to positive outcomes and successful business results Perform other duties as directed by the functional manager Serve as Local/External Lab Lead for global studies, which includes being the primary local lab contact for customers, CRAs, and site monitors Acts as resource for researchers, Medical Technologist, Clinical Laboratory Scientists, Medical Laboratory Technicians and/or Assistants in the technical area to resolve data questions Provides scientific and technical advice and communicates appropriately to ensure delivery to the customer's satisfaction, on time and within budget Develops formal documentation for position as required by operating procedures, many of which outline specific requirements for managing local lab data Manages the delivery of projects through full data management study life-cycle, from setup to lock Supports the identification and resolution of service level issues, as well as the proactive development of contingency plans to mitigate laboratory risk Works with customers, scientific team, data managers and internal team members to manage issue escalation, workload projections, and provide technical expertise Interacts and communicates with internal and external customers to ensure that timelines are met and that data is delivered following company guidelines and regulatory compliance With guidance, manages project timelines and quality issues, and identifies and justifies out-of-scope client requests Assists internal team with data entry, review and validation of laboratory reports, and serves as back-up contact when needed Performs comprehensive quality control and edit check procedures Supports service delivery with comprehensive process and technical expertise in executing projects which includes identifying and resolving issues. Effectively works on corrective and develop preventive action plans Qualifications Bachelor's Degree in Medical Technologist or Clinical Laboratory Scientist degree with clinical laboratory experience OR Computer Science with Software Configuration and Validation experience 2-3 years of experience in Data Management and SAS Programming. Requires basic knowledge of SAS Programming and Data Management procedures obtained through prior work experience or education. Equivalent combination of education, training, computing qualification and experience. Good customer-focus perspective with skill to guide customer communications and customer management. Good attention to detail to anticipate, address and/or escalate issues, with aptitude to embrace and be conduit for change. Good project and task management capabilities and ability to manage multiple projects and tasks simultaneously. Effective problem solving skills as well as ability to proactively identifying process improvements which reduce operational costs and maintain quality. Quality conscious with high degree of ethics and integrity carrying out duties in accordance to laws, regulatory standards, and with company policies and procedures. Proficiency in Windows operating systems (user-level skills), Microsoft Office applications. Good understanding of medical, clinical research, and Lab Data Management process and terminology. Working knowledge on various regulatory requirements such as FDA, ICH, ISO HL7, and GLP (Good Laboratory Practices). IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Our MedTech Device Field Collection Associate experiences a unique opportunity for collecting reprocessed medical equipment in a hospital. You will be working with surgical, non-invasive and vascular equipment within areas of the hospital such as Operating Rooms and Sterile Processing Departments. This is a great opportunity for you to gain medical experience!  You will have a flexible schedule and an opportunity to grow and expand into new opportunities while earning supplemental income and learning about the medical device industry.   What you will be doing in the role: Visit assigned hospitals weekly to collect products to be reprocessed Package and ship product to client manufacturing plant Document and log daily collections totals Notify the local Sales team of shipping supply needs Appropriate PPE is provided to all employees prior to the start of assignments. Available to work approximately 12-15 hours a week Training for this role will be provided and is paid Job Requirements:   An active and unrestricted driver license is required for this position  Minimum High school diploma or equivalent Reliable vehicle for transportation Must be comfortable with basic software programs and Microsoft operating system  Excellent customer service skills and strong attention to detail Ability to lift 30-50 lbs Ability to clear hospital vendor credentialing requirements, including proof of vaccination status, required  Travel Requirement: Travel locally for up to 2-3 hours to support customer needs Must have an active driver license and a personal vehicle to use for job related assignments Travel time is paid, as is mileage Preferred Attributes: Experience in healthcare, general labor, warehouse or customer service, is beneficial for this position. Ability to work independently in customer settings with minimal supervision. IQVIA MedTech CFS takes the approach to helping customers drive healthcare forward in this challenging and fast-paced environment. We help customers accelerate results, improve patient outcomes, and unleash new opportunities. Benefits: This position is not eligible for our Medical Benefits. Vaccine/Immunization/Hospital Credentialing Requirement: A required function of this job requires individuals to enter various healthcare facilities.  Thus, upon selection, individuals must complete healthcare facility credentialing process.  To obtain credentials, individuals must meet the immunization requirements specified by the facility.  Individuals are typically required to have completed/up to date: Measles, Mumps & Rubella vaccine, Varicella (chicken pox) vaccine, Negative Tuberculosis (TB) Test, Tetanus, Diphtheria & Pertussis (Tdap) vaccine, Hepatitis B vaccine, Influenza vaccine (seasonal), and COVID-19 vaccine primary series (heavily enforced by most facilities, some require booster(s)). Please note, IQVIA complies with all applicable laws regarding reasonable accommodations or exemptions for religious, medical, or other legally protected reasons, however, our client’s requirements may supersede this.  *Please note: No relocation is being offered for this role. Candidate must live locally to be considered. Due to the nature of this role, it is not eligible for Visa sponsorship. LFT1 IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. The potential base pay range for this role is $20.00 - $22.00 per hour. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

Job OverviewActs as Lead Medical Writer on most types of writing projects. Prepares assigned documents in accordance with IQVIA Standard Operating Procedures (SOPs) and customer requirements as well as to the agreed timelines. Performs Senior Review of straightforward medical writing deliverables. Negotiates timelines and discusses/resolves customer comments.Provides written and verbal feedback to junior staff, and to customers when appropriate. Keeps abreast of current medical and/or technical writing/regulatory knowledge, including Good Clinical Practice (GCP), along with developments and advances in drug development/medical and/or technical writing. Essential Functions Take a leading role in preparing assigned documents, including, but not limited to, confirming the scope of the task, confirming templates and specifications, negotiating and adhering to timelines, organizing document reviews, communicating directly with the customer. Plan and organize workload for assigned projects and tasks: identify project needs, track timelines and implement customer requests. Lead meetings on more challenging topics independently. May present on standard Medical Writing processes at full-service bid defense meetings. Assist in the training and development of junior staff, either formally as an assigned mentor or ad hoc for local colleagues or others. May develop and deliver training to the global team on a topic he/she has specific expertise in. May input into and deliver presentations on Medical Writing to other IQVIA groups. May act as Project Manager for a more complex but single Medical Writing project which includes Project Finance/Invoicing responsibilities. Complete project finance activities, including monitoring and forecasting budgeted hours. Propose, review and approve budgets and costings for routine projects, including estimation of hours needed for Medical Writing tasks. May take on a small customer lead role or assist an established partnership lead in their role. May represent region or site on a Medical Writing initiative or cross-functional initiative. Facilitates and brainstorms the identification of new ideas. May represent Medical Writing at a general capabilities audit. Qualifications Bachelor's Degree Bachelor's Degree in life sciences related discipline or related field Master's Degree Master's Degree in life sciences related discipline or related field   Ph.D. Ph.D. in life sciences related discipline or related field Pref Typically requires at least 5 years of highly relevant experience and related competency levels. Req In-depth knowledge of the structural and content requirements of clinical study reports, protocols, and similar documents and ability to identify deficiencies, errors, and inconsistencies in a protocol or report. Good understanding of common statistical methods used in clinical trials and/or interpretation of their results. Ability to effectively review a statistical analysis plan and to identify deficiencies, errors, and inconsistencies in statistical output Ability to integrate, interpret, and summarize data from a variety of sources in a clear and concise manner. Significant experience as a lead writer in preparing CSRs and protocols, with consistently positive feedback from customers and colleagues. In depth knowledge of drug development, medical writing, and associated regulations. Good understanding of statistical principles and of medical terminology across a range of therapeutic areas. Excellent written and oral communication skills including grammatical/technical writing skills. Excellent attention to detail and accuracy. Confident and effective communication and negotiation skills with customers and project managers. Able to deliver difficult messages in constructive manner. Demonstrates initiative and sound judgement when faced with less familiar project/document situations or challenges. Demonstrated abilities in collaboration with others and independent thought. Demonstrates confidence and maturity in most routine medical writing situations. Demonstrates good judgement in requesting input from senior staff. Ability to establish and maintain effective working relationships with coworkers, managers and customers. Ability to effectively manage multiple tasks and projects. Ability to proactively evaluate risks and potential issues and seek solutions and discuss appropriately with colleagues and customers. Must be computer literate. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

What is Decision Analytic Modelling in Healthcare? When a new medicine, vaccine or medical technology is developed, healthcare systems globally face decisions on whether to fund it, and for whom. These decisions involve complex trade-offs: How effective is the treatment compared to current alternatives? What are the costs over a patient's lifetime? How does it affect quality of life?  Decision analytic modelling in healthcare is the discipline that helps answer these questions. Using quantitative models (e.g., decision trees, Markov models, survival-based simulations and other mathematical frameworks) we synthesise clinical evidence, cost data and patient related outcomes to project the long-term value of healthcare interventions. Our models inform pricing, reimbursement and access decisions made by payers, health technology assessment (HTA) bodies, and regulatory authorities across the globe. Prior Experience If you have a strong quantitative background – whether in mathematics, statistics, engineering, economics, biomedical sciences or a related discipline – and enjoy building structured quantitative models, working with data and solving complex analytical problems, this role as an Analyst - Health Economic Modeller offers an opportunity to apply those skills in a meaningful real-world context, helping patients to access treatments they need. No prior experience in health economic modelling is required. This is an entry-level role with structured training opportunities designed to build technical depth in decision analytic modelling for healthcare and develop subject matter expertise. Within IQVIA’s Global Health Economic Modelling Team, as part of a structured onboarding program, you will be provided with comprehensive training in health economic modelling methods, HTA processes and the life sciences industry. The Role As an analyst, you will work flexibly across health economic modelling projects, gaining exposure to a broad range of model types, therapeutic and disease areas, and healthcare systems. The primary focus of this role is on supporting the development of de novo models and adaptations of existing models that support evidence-based healthcare decision-making, although there is flexibility to work on other types of projects should the opportunity arise. Analysts support the team in project delivery, with the opportunity to also support business development. Key Responsibilities Develop decision analytic models – contribute to the design and programming of quantitative models (e.g. decision trees, Markov models, partitioned survival models) in Microsoft Excel (and VBA) and R, with support and guidance from more senior team members Conduct statistical analyses – perform basic statistical analyses (descriptive statistics, regression analysis, survival analysis) using R to generate inputs for decision analytic models Produce project deliverables – develop model analysis plans, technical reports, user guides and slide decks with guidance from the project team, ensuring deliverables meet quality standards and deadlines Support the Centre of Excellence – contribute to the development of global modelling materials, processes, methodology, and templates as part of the Global Health Economic Modelling Centre of Excellence Support thought leadership – assist in the dissemination of findings through conference abstracts, posters, articles and presentations, and contribute to internal initiatives for innovative methodological approaches Build knowledge of the team's offerings – develop familiarity with the full range of the team's modelling and broader health economics offerings to support business development opportunities as they arise The demand for IQVIA's decision analytic modelling offerings has seen dramatic increases over the past years and will continue to expand in response to evolving analytical, software and regulatory processes globally. The role is based in either Greece, Portugal or South Africa, with flexibility regarding frequency of office and home working. The Successful Candidate We are looking for proactive individuals with strong quantitative and problem-solving skills who are excited by the prospect of applying analytical modelling to real-world healthcare challenges. You do not need a background in health economic modelling – we are looking for people who naturally approach problems through structured quantitative thinking, are comfortable with numbers and data, and are eager to learn how their technical skills can be applied in a new and impactful domain. Candidates should have the technical aptitude to work with spreadsheet-based models and statistical software, combined with a curiosity about how data-driven analysis can support decision-making. The tenacity to work through complex, iterative modelling tasks and deliver to a high standard is a quality we particularly value. The role requires analysts to work flexibly across multiple projects. A baseline level of organizational skills and time management is important to ensure that analysts can complete their assigned work to meet deadlines at a consistently high standard, while maintaining a good work-life balance. The ideal applicant should have apt interpersonal skills and the ability to establish relationships with both internal team members and clients. As such, fluency in English is essential. The ability to demonstrate this through slide deck development, report writing, and presentations is essential. Qualifications IQVIA are focused on selecting candidates with passion and drive to be successful in the industry. There is no specific profile that is conducive to success, and we recruit individuals from a variety of backgrounds to create a well-rounded team. If you are motivated, have a curiosity about healthcare, and strong analytical skills we encourage you to apply. The list below should be viewed as a guide rather than a checklist. Essential: BSc or MSc in a quantitative or technical discipline (e.g., mathematics, actuarial sciences, physics, statistics, engineering, biomedical sciences, operations research, or related fields). Degrees in health economics are welcome but not required Proficiency in Microsoft Excel and at least one programming or statistical software environment (e.g., R, MATLAB, Python, or similar) Basic statistical literacy (e.g., descriptive statistics, regression analysis, etc.) Experience building or working with quantitative models (e.g., simulation models, optimization models, statistical models, engineering models, etc.)  whether in academic projects, internships, or coursework Strong written and verbal communication skills with fluency in English language Self-motivated with a strong desire to learn quickly and independently Tenacity to work through complex, iterative analytical tasks Excellent attention to detail and ability to check own work Strong time management and organizational skills, and flexibility to work in a fast-paced, multi-project environment Keen to work as a member of a diverse, multi-cultural team Desirable: MSc in any of the above disciplines or in health economics Dissertation or thesis project involving quantitative modelling or data analysis Experience with or interest in healthcare, life sciences, and the pharmaceutical, biotechnology and medical device industry Familiarity with decision analytic modelling concepts (e.g. decision trees, Markov models, cost-effectiveness analysis) Familiarity with VBA or advanced Excel functionality, including contemporary Excel functions (e.g. LET, LAMBDA) Familiarity with survival analysis or time-to-event analysis concepts Knowledge of health technology assessment (HTA) processes or healthcare reimbursement systems Please submit your CV in English.  The Company and the Team IQVIA IQVIA is a fast-growing and highly successful business, delivering data-driven insights and measurable impact for clients across the global life sciences ecosystem. Leveraging access to some of the world’s most comprehensive healthcare data, advanced analytics and research capabilities, IQVIA experts design and deliver innovative, technology-enabled evidence programs to support decision-making across the product lifecycle. Commercial Solutions Excellence Centres (CSEC) CSEC is a global function that centralizes service delivery across IQVIA’s core commercial offerings. It brings together global and regional teams, building scale to improve quality, efficiency, and innovation. By combining diverse talent with automation and AI, CSEC accelerates commercial excellence worldwide, working closely with global functions and regional business units to continuously improve delivery performance Global Health Economics and Health Technology Assessment (HE/HTA) The Global HE/HTA team brings together multidisciplinary experts in health economics, evidence synthesis, literature review, value communication, and health technology assessment across CSEC. The team works with organizations that fund, assess, regulate and implement healthcare, including the top 20 global pharmaceutical, biotechnology and medical device companies, as well as payers, health technology assessment bodies and regulatory authorities. The Global HE/HTA team supports clients in designing and executing evidence generation strategies, evaluating clinical and economic value of their assets, and communicating robust value narratives to a diverse range of stakeholders, spanning the full spectrum of therapeutic and disease areas. Our diverse mix of clients, the breadth of disease areas, as well as increasing access to novel data sources and methodologies provide a constant and rewarding challenge for our people. For more information about our company please visit our website: https://www.iqvia.com/ IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com. IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. At IQVIA, we believe that diversity, inclusion, and belonging empower our mission to accelerate innovation for a healthier world. We create a culture of belonging by valuing the perspectives of all talented employees worldwide and providing them with the opportunity to power smarter healthcare for everyone, everywhere. When our talented employees bring their authentic selves and their diverse experiences to work, they enable us to accomplish extraordinary things. Multifaceted thought processes spark innovation. Multi-talented collaboration harnesses innovation to deliver superior outcomes. Likewise, as part of this culture, IQVIA is committed to ensuring effective equality between women and men, integrating it as a strategic principle in its corporate and human resources policies.

Our MedTech Device Field Collection Associate experiences a unique opportunity for collecting reprocessed medical equipment in a hospital. You will be working with surgical, non-invasive and vascular equipment within areas of the hospital such as Operating Rooms and Sterile Processing Departments. This is a great opportunity for you to gain medical experience!  You will have a flexible schedule and an opportunity to grow and expand into new opportunities while earning supplemental income and learning about the medical device industry.   What you will be doing in the role: Visit assigned hospitals weekly to collect products to be reprocessed Package and ship product to client manufacturing plant Document and log daily collections totals Notify the local Sales team of shipping supply needs Appropriate PPE is provided to all employees prior to the start of assignments. Available to work approximately 12-15 hours a week Training for this role will be provided and is paid Job Requirements:   An active and unrestricted driver license is required for this position  Minimum High school diploma or equivalent Reliable vehicle for transportation Must be comfortable with basic software programs and Microsoft operating system  Excellent customer service skills and strong attention to detail Ability to lift 30-50 lbs Ability to clear hospital vendor credentialing requirements, including proof of vaccination status, required  Travel Requirement: Travel locally for up to 2-3 hours to support customer needs Must have an active driver license and a personal vehicle to use for job related assignments Travel time is paid, as is mileage Preferred Attributes: Experience in healthcare, general labor, warehouse or customer service, is beneficial for this position. Ability to work independently in customer settings with minimal supervision. IQVIA MedTech CFS takes the approach to helping customers drive healthcare forward in this challenging and fast-paced environment. We help customers accelerate results, improve patient outcomes, and unleash new opportunities. Benefits: This position is not eligible for our Medical Benefits. Vaccine/Immunization/Hospital Credentialing Requirement: A required function of this job requires individuals to enter various healthcare facilities.  Thus, upon selection, individuals must complete healthcare facility credentialing process.  To obtain credentials, individuals must meet the immunization requirements specified by the facility.  Individuals are typically required to have completed/up to date: Measles, Mumps & Rubella vaccine, Varicella (chicken pox) vaccine, Negative Tuberculosis (TB) Test, Tetanus, Diphtheria & Pertussis (Tdap) vaccine, Hepatitis B vaccine, Influenza vaccine (seasonal), and COVID-19 vaccine primary series (heavily enforced by most facilities, some require booster(s)). Please note, IQVIA complies with all applicable laws regarding reasonable accommodations or exemptions for religious, medical, or other legally protected reasons, however, our client’s requirements may supersede this.  *Please note: No relocation is being offered for this role. Candidate must live locally to be considered. Due to the nature of this role, it is not eligible for Visa sponsorship. LFT1 IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. The potential base pay range for this role is $20.00 - $22.00 per hour. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

Job OverviewProvide strategic leadership at customer account level for multiple large projects, as assigned by senior management team. Act as Sponsor's primary point of contact throughout project duration for local and globally scoped deliverables (programs) with single/multiple Lifecycle Safety functions. Line management responsibilities for assigned Customer Delivery Leadership (CDL) staff aligned to work on account(s) owned by the Customer Team Management (CTM). Collaborate with global management team to develop and implement strategic initiatives and ensure global consistency.Essential Functions Work with Sales and Proposals to ensure rapid, seamless, tailored responses to opportunities. Drive business growth by improving customer loyalty through enhanced customer relations, service delivery excellence and excellent customer communication.Collaborate in the definition of customer-centric, account management strategies and provide oversight of their implementation within assigned account(s) i.e. solicitation of repeat business; identification of new business opportunities developing to RFPs; assist in contribution of customer centric, strategic focus to proposal development process; assist in transforming customer relationships to partnership level; establish mutually agreed working practices with customer for standardization implementation across projects/programs; contribute to strategic planning, assist in creative solutions and ongoing process improvements to meet anticipated future customer needs; provide customer feedback; status reports.Works with Lifecycle Safety service operations constructively in a matrix framework to achieve project and customers deliverables.Lead and contribute to Global initiatives and will work in close collaboration with Service Operations (SO) and Lifecycle Safety Infrastructure. Assist in the implementation and support of customer managed decisions as determined under guidance by senior management.Impart specialist expertise in CDU aligned specialist areas, as well as applying them across LSM and SO.Lead by example bid defenses; client meetings; attend investigator meetings, and present as required.Maintain ongoing project communications with internal and external project stakeholders.Manage scope and budget review and finalization with sponsors ensuring program financial targets are met.Accountable for oversight of Lifecycle Safety performance for projects/programs on assigned account(s) to include customer interface and communications; customer deliverable and realization/profitability; service integration and technical solutions.Provide effective senior representation of Lifecycle Safety in high visibility forums e.g. joint IQVIA-Sponsor steering Committees, GOH teams, cross-functional project reviews.Effectively contribute to sales activities across other accounts and Customer Delivery Management as needed.Provide historical perspective and input on clients and processes. Provide input on the success or failure of previous initiatives and appropriately field concerns. Hold at least bi-monthly meetings with direct reports to discuss, at a minimum: project status, including timelines, delivery updates, financial aspects of the group or project, and potential risks, associated mitigation and support required; status of any initiatives that they may be involved in; the team's utilization rates; the direct report's training and other administrative obligations, such as Standard Operating Procedures (SOPs) and corporate training mandates; personnel issues; and career or training objectives.Create and implement plans for measuring and improving employee engagement ensuring global consistency. Maintain open and regular communication with direct reports to ensure a supportive working environment.Efficiently conveying messages from leadership to direct reports and teams, as well as effectively communicating issues and opportunities up to leadership.Might be needed to serve as the designated substitute or alternatively ensure coverage is in place for direct reports during their absence or in case of turnover.Prepare, present and respond in bid defense meetings and discussions. May input into more complex requests for information (RFIs) or requests for proposal (RFPs). Liaise with Business Development to give timely inputs regarding the feasibility of all new proposals going out to clients.Contribute at IQVIA internal cross-functional project team meetings interfacing with other functional leads customer project status meetings and oversight group meetings. Subject Matter Expert (SME) Meetings, as appropriate.Qualifications Bachelor's Degree Health science or other directly related field 8 years' clinical research experience in a Contract Research Organization or Pharmaceutical company combining 5 years of Lifecycle Safety experience(Pharmacovigilance, CEVA, Medical Information, Safety Publishing, Risk Management, etc) and 3 years' line management experience or equivalent combination of education, training or experience In depth knowledge and understanding of Lifecycle Safety service lines; willingness to increase knowledge across Lifecycle Safety service lines and develop new skills.Strong business acumen; financial management and budgeting skills.Proven Staff management skills, strong leadership, motivational and influencing skills.Strong project management; strategic planning; delegation and organisational skills. Proven ability to work on multiple projects and manage competing priorities.Confident in raising and discussing sensitive topics without management intervention and in communicating effectively with senior levels of management in both IQVIA and customer organizations.Demonstrated ability to remain calm and assertive yet diplomatic in more challenging interactions with customers and colleagues.Excellent communication (both verbal and written), presentation and negotiation skills.Ability to establish and maintain effective working relationships with coworkers, direct reports, managers, and customers at a senior level.Autonomous independent decision-making; problem solving and judgment skills.Strong customer focus; account and alliance management and experience in customer contracting models.Proven ability to professionally network; present and lead at meetings/ teleconferencesAbility to achieve results through communication, facilitation, negotiations in a matrix service delivery environment with shared responsibilities.Demonstrate excellent flexibility; self-motivation; creativity; innovation and solutions driven approachDemonstrates financial awareness. Promotes good practices to manage financial performance.Strong ownership skills: take initiative and move forward with limited guidance.IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. The potential base pay range for this role, when annualized, is $98,200.00 - $273,200.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

Senior Site Activation Coordinator Country Site Activation – CSA South Africa Home-based Make an impact on patient health! IQVIA’s Global Site Activation Team of 2000 employees, drives best in class site and customer experience, with industry leading outcomes. We keep the patient at the forefront; ‘Always Impatient for the Patient’ and we excel in our collaboration with our external/internal customers.   IQVIA’s Country Site Activation team are a global network who identify and activate sites to the highest quality to ensure patients on Clinical trials have access to safe and effective medication.  We are leaders in innovation and first to new technologies, meaning a vast amount of career development opportunities are available. Job Overview: As a Site Activation Coordinator, under general supervision, you will perform tasks at a country level associated with site activation activities. These activities will be in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. You will perform feasibility, site activation and some maintenance activities in assigned studies for investigative sites, according to applicable regulations, SOPs, and work instructions, working closely with the Site Activation Manager, Project Management team, and other departments as necessary.  Coupled with reviewing documents for completeness, consistency, and accuracy, under guidance of senior staff, you will prepare site documents, review, track and follow up the progress, the approval and execution of required documents such as questionnaires, CDAs, regulatory, ethics, Informed Consent Form, and Investigator Pack release documents.  You will also support the updating and maintenance of internal systems, databases, tracking tools, timelines, and project plans with accurate and complete project specific information.  Requirements:  Bachelor’s Degree in Life Science or related field   Minimum 2 years’ work experience; 1+ years in healthcare or similar  Good interpersonal, communication and organizational skills to establish and maintain effective working relationships with co-workers, managers and sponsors Ability to work on multiple projects Join IQVIA and let’s create a healthier world together: Exposure across 21 Therapeutic Areas  Be part of a global team who operate across 141 locations  Exposure across a variety of studies and projects  Access to new, innovative technologies  Work within a collaborative and vibrant environment  Own your career!  Unleash your potential! It takes passion to make the extraordinary possible for patients. Our culture of innovation and collaboration enables us to explore new possibilities and help improve health around the world. When you join our diverse, global team, you’ll harness the power of unparalleled data, advanced analytics, cutting-edge technologies, and deep healthcare and scientific expertise to drive healthcare forward. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Job OverviewPerform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include maintenance activities.Home Based role for an applicant with Romanian submissions experience to EC and RA and ICF adaptation. Romania language fluency required and additional languages beneficial.   Essential Functions Under general supervision, serve as Single Point of Contact (SPOC) in assigned studies for investigative sites, Site Activation Manager (SAM), Project Management team, and other departments as necessary.Ensure adherence to standard operating procedures (SOPs), Work Instructions (WIs), quality of designated deliverables and project timelines.Perform start up and site activation activities according to applicable regulations, SOPs and work instructions.Distribute completed documents to sites and internal project team members.Prepare site regulatory documents, reviewing for completeness and accuracy.Ensure accurate completion and maintenance of internal systems, databases and tracking tools with project specific information.Review and provide feedback to management on site performance metrics.Review, establish and agree on project planning and project timelines.Ensure monitoring measures are in place and implement contingency plan as needed.Inform team members of completion of regulatory and contractual documents for individual sites.Review, track and follow up the progress, the approval and execution of documents, regulatory, ethics, Informed Consent Form (ICF), and Investigator Pack (IP) release documents, in line with project timelines.Provide local expertise to SAMs and project team during initial and on-going project timeline planning.Perform quality control of documents provided by sites.May have direct contact with sponsors on specific initiatives. QualificationsBachelor’s Degree in life sciences or a related field and 3 years’ clinical research or other relevant experience; or equivalent combination of education, training and experience. In-depth knowledge of clinical systems, procedures, and corporate standards.Knowledge and ability to apply GCP/ICH and applicable regulatory guidelines.Knowledge of applicable regulatory requirements, including local regulations, , SOPs and company’s Corporate Standards.Understanding of regulated clinical trial environment and knowledge of drug development process.IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

IQVIA™ – The Human Data Science Company™ – ist ein führender, globaler Anbieter von zukunftsweisender Analytik, Technologielösungen und klinischer Auftragsforschung. IQVIA unterstützt Life Science Unternehmen, Verbände, Institutionen, Kostenträger und weitere Akteure im Gesundheitswesen darin, bessere Ergebnisse in der Gesundheitsversorgung zu erzielen. Werden Sie Teil unserer Community von rund 86.000 Mitarbeiterinnen und Mitarbeitern in über 100 Ländern, die sich dafür einsetzen, das Potenzial von Human Data Science Wirklichkeit werden zu lassen! Ganz gleich, in welche Rolle Sie bei IQVIA einsteigen, es erwartet Sie ein offenes, innovationsfreudiges Umfeld, in dem Sie sich viel bewegen können. Finden Sie heraus, wie Sie Ihre Talente und Ihre Leidenschaften bei IQVIA einbringen können. Im Bereich Commercial Engagement Services (CES) arbeiten wir eng mit unseren Life Sciences-Kunden zusammen und unterstützen sie mit flexiblen Vertriebs- und Personallösungen für nachhaltigen Erfolg am Markt. Dies umfasst insbesondere die Rekrutierung, das Training und die Steuerung des Vertriebsteams in Dienstleistungsprojekten bzw. in Arbeitnehmerüberlassung. Dabei differenzieren wir uns über integrierte Projektansätze entlang des IQVIA Lösungsportfolios, die wir individuell an die Kundenbedürfnisse anpassen und aus einer Hand anbieten. Komm in unser Team! Für einen bundesweiten Teamaufbau suchen wir Pharmareferenten (m/w/d) und Pharmaberater (m/w/d) zum nächstmöglichen Zeitpunkt mit Engagement und Begeisterungsfähigkeit. Im Gebiet: Aachen, Bonn, Euskirchen Das sind Deine Aufgaben: Durch die intensive Betreuung ausgewählter Ärzte förderst Du die Empfehlung Deiner Präparate und trägst so maßgeblich zum Unternehmenserfolg bei. Du setzt als Experte auf der Basis Deines Fachwissens Beratungsstrategien erfolgreich um und überzeugst so Deine Ansprechpartner. Du findest mit Deinen Gesprächspartnern innovative Therapiekonzepte zum Wohle des Patienten und trägst somit zur Gesundheit und dem Patientenwohl bei. Das wünschen wir uns von Dir: Du hast bereits Erfahrung als Pharmaberater oder Pharmareferent in verschiedenen Indikationen gesammelt. Wir geben auch Neueinsteigern mit entsprechender Qualifikation nach § 75 AMG die Chance mit IQVIA ihre Karriere zu starten. Du verfügst über eine Naturwissenschaftliche Ausbildung (idealerweise Hochschulabschluss) oder Ausbildung zum Geprüften Pharmareferent (m/w/d) gemäß §75 AMG Als durchsetzungsstarke, vertriebsorientierte Persönlichkeit und erfahrener Netzwerker verstehst Du es, dich und Deine Ansprechpartner zu begeistern. Du möchtest etwas bewegen – für Dein Präparat, für dich selbst und vor allem für betroffene Patienten. Ausgeprägte kommunikative Fähigkeiten sowie die Bereitschaft, eigenverantwortlich und ergebnisorientiert zu arbeiten. Du verfügst über sehr gute Deutsch-Kenntnisse und bist technik-affin Darauf darfst du Dich freuen: In unserer Arbeitskultur legen wir großen Wert auf Zusammenarbeit, Respekt und gegenseitige Unterstützung. Wir fördern eine Umgebung, in der sich jeder willkommen und wertgeschätzt fühlt. Offene Kommunikation und Transparenz sind für uns essenziell, um Vertrauen und ein starkes Gemeinschaftsgefühl zu schaffen. Ein attraktives Gehaltspaket plus Kundenprämien, vielfältige Corporate Benefits, betriebliche Altersvorsorge sowie 24/7 Unfallversicherung (auch für den privaten Bereich) und exklusive private Krankenzusatzversicherungen Ein top ausgestatteter Firmenwagen verschiedener Premiumanbieter mit uneingeschränkter Privatnutzung (ohne Zuzahlung) und mit Wahlmöglichkeit des Modells   Eine moderne IT-Ausstattung für Deinen modernen digitalen Arbeitsplatz Unser unbefristetes IQVIA Arbeitsverhältnis bietet Sicherheit und eine langfristige Perspektive Wir bieten u.a. tarifliche Sonderurlaubstage, Umzugszuschuss bei betrieblich bedingtem Wechsel deines Wohnorts Eine hohe Übernahmequote durch unsere Kunden ermöglicht Dir den Karrierestart bei zukunftsweisenden und führenden Unternehmen der Pharmabranche und Medizintechnik-Branche Vielfältige und individuelle Weiterentwicklungsmöglichkeiten auch innerhalb von IQVIA (z.B. Führung, Key Account Management, Projektmanagement und vieles mehr) Wir begleiten Dich während Deiner Bewerbungsphase durch individuelle Betreuung/Vorbereitung bis zur Einstellung und auch darüber hinaus während des Beschäftigungsverhältnisses Unser Kunden-Netzwerk reicht vom Start-up Unternehmen bis zum Global Player. Gemeinsam mit Dir finden wir den richtigen Job für Dich! Starte Deine Karriere mit IQVIA! Dein besonders schneller Draht zu uns: Kandidaten-Hotline: 0621-84508113 oder sende uns gerne direkt Deine Bewerbung per Mail an: [email protected] , besser noch lade deinen Lebenslauf direkt nach deiner Registrierung in Workday hoch. Hier der Link: Workday #LI-CES #LI-DNP #LI-SS2 #Pharmaberater #Biologie #Chemie #Pharmareferent #BTA #CTA #PTA #MTA #Oecotrophologie #Pharmazie #Pharma-Außendienst IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Job Overview The Global Study Associate is a member of the extended global study team supporting delivery of clinical studies within BioPharmaceuticals Clinical Operations, Study Management to time, cost and quality.The GSA supports delivery of global clinical studies from study set-up through maintenance, close-out and study archiving. The GSA supports the Global Study Director (GSD), Global Study Associate Director (GSAD) and/or Global Study Manager (GSM) with coordinating activities, ensuring quality and consistency. The GSA supports with administration & systems and with other delegated aspects of clinical study execution in accordance with applicable clinical trial regulations (ex. ICH-GCP). Essential Functions Support GS(A)D and GSMs by completing delegated study work. May work across many different studies and delivery models concurrently.• Initiate and lead the set-up of the electronic Trial Master File (eTMF). Maintain and close the eTMF to ensure compliance to International Conference of Harmonisation Guidelines for Good Clinical Practice (ICH/GCP) and client's SOPs.• Interact/collaborate with internal staff and external stakeholders in collection of regulatory and other essential documents.• Contribute to electronic applications/submissions in ANGEL by creating and managing clinical regulatory documents according to the requested technical standards and supporting effective publishing and delivery to regulatory authorities. Proactively plan and collate the administrative appendices for the CSR.• Initiate and maintain production of study documents, ensuring template and version compliance per study specific requirements.• Set-up, populate and accurately maintain information in client's tracking and communication tools and support team members in the usage of these tools.• Support the set-up, maintenance and close-out of Clinical Trial Transparency (CTT) activity in PharmaCM, coordinating with relevant stakeholders to fulfil client's compliance and meet the regulatory authority needs.• Support the GS(A)D with tracking, reconciliation and follow-up of the study budget/payments in relevant systems.• Contribute to application, coordination, supply and tracking of study materials and equipment. Contribute to collection of study supplies, if required, at the study close-out.• Coordinate administrative tasks and logistic support throughout the conduct of the study, audits and regulatory inspections, according to company policies and SOPs.• Prepare, contribute and distribute presentation material for meetings, newsletters and websites. Qualifications • Education in medical or biological sciences or discipline associated with clinical research preferred• Proven organizational and analytical skills• Previous administrative training/experience• Excellent verbal and written communication in English• Demonstrate ability to work independently, as well as in a team environment• Ability to prepare presentation materials• Demonstrate professionalism and mutual respect• Willingness and ability to train others on study administration procedures• Experience in clinical study lifecycle Please note this role is not eligible for the UK visa sponsorship. Please note: due to sponsor requirements for the role only candidates based in the listed location/s will be considered. Any applications from candidates based outside of these locations will not be considered. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. The potential base pay range for this role, when annualized, is 80.500,00 zł - 190.900,00 zł. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

Job Overview The Global Study Manager is a member of the extended global study team supporting delivery of clinical studies within BioPharmaceuticals Clincal Operations, Study Management to time, cost and quality, from Clinical Study Protocol (CSP) development through study set-up, maintenance, close-out, development of Clinical Study Report (CSR) to study archiving.The GSM works cross-functionally with internal and external partners to deliver delegated aspects of the clinical study in accordance with Global Study Director (GSD) or Global Study Associate Director (GSAD) in delegated aspects of clinical study execution in accordance with the Delivery Model. Essential Functions In partnership with client's team,• Leads/contributes to the preparation of delegated study documents (e.g., Informed Consent Form, master Clinical Study Agreement etc), and external service provider related documents (specifications, study specific procedures, descriptions, presentations etc.).• Maintains and facilitates interactions with internal functions and external functions including the CROs and other external service providers to ensure an efficient study delivery to time, costs and quality objectives.• Contributes to the planning and conduct of internal and external meetings (e.g., Investigators’/Monitors’ meeting).• Ensures the supply of Investigational product and study materials by liaising with Clinical Supply Chain or external service providers as appropriate.• Proactively contributes to risk and issue identification, development of mitigation and/or action plans for identified risks and issues.• Ensures that all study documents in scope of GSM’s responsibilities are complete and verified for quality in Trial Master File.• Supports GSD and/or GSAD with budget management, such as external service provider invoice reconciliation.• Adheres to global clinical processes, procedural documents, applicable Quality & Compliance manual documents and international guidelines such as ICH/GCP to ensure study is inspection ready at all times.• Supports GSD and/or GSAD with overall project management as per agreed delegation.• For outsourced studies, supports GSD and/or GSAD in management of the CRO Project Manager to ensure study delivery according to agreed timelines, budget and quality standards, while ensuring that the appropriate level of oversight of the CRO is maintained and documented throughout the lifecycle of the study, in accordance withInternal BioPharmaceuticals Clinical Operations Job Descriptionrelevant client's SOPs and guidelines (e.g., description of services and transfer of obligations)• Take on assignments on non-drug project work in process improvements and/or leading improvement projects as discussed and agreed upon with their manager Qualifications • University degree (or equivalent), preferably in medical or biological sciences or discipline associated with clinical research.• Relevant experience from within the pharmaceutical industry or similar organization or academic experience, preferably of at least 3 years.• Knowledge of clinical development / drug development process in various phases of development and therapy areas• Excellent knowledge of international guidelines ICH/GCP• Excellent communication and relationship building skills, including external service provider management skills• Good project management skills• Demonstrated ability to collaborate as well as work independently• Demonstrated leadership skills• Computer proficiency, advanced computer skills in day-to-day tasks• Excellent verbal and written communication in English  Please note this role is not eligible for the UK visa sponsorship. Please note: due to sponsor requirements for the role only candidates based in the listed location/s will be considered. Any applications from candidates based outside of these locations will not be considered. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. The potential base pay range for this role, when annualized, is 171.500,00 zł - 404.600,00 zł. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

IQVIA is growing! Hiring multiple Clinical Data Management (CDM) Leads across our FSP (Functional Service Provider) and Traditional (Sponsor-Agnostic) delivery models. Apply now and have your resume considered for Lead Data Manager opportunities across multiple teams - allowing us to match you with the best-fit project and client environment for your experience and interests!  IQVIA is seeking experienced Clinical Data Management Leads to oversee end-to-end data management delivery for global clinical trials. You’ll ensure quality, accuracy, and compliance while leading cross-functional teams that help bring new therapies to life. This is a remote/WFH position with all necessary equipment provided.What You’ll Do Lead data management for complex, global clinical trials from study setup to database lock.Serve as the main client contact for all data management deliverables.Oversee SAE, PK, and external data reconciliation and database deployment.Manage timelines, budgets, and resource allocation to meet customer expectations.Mentor junior data management staff and promote best practices.Drive process improvements and ensure regulatory and SOP compliance.Who We’re Looking For Ideal candidates will have.... Bachelor’s degree in life sciences, health, clinical, biological, or mathematical field.No less than 10 years of direct clinical data management experience, with 5+ years in a Lead Clinical Data Management role.Your previous roles/job titles may include Clinical Data Manager, Senior Clinical Data Manager, Lead Data Manager, Principal Data Manager, and/or Data Management Project Manager.Proven success managing large global studies (1000+ patients).Expertise with Medidata Rave, Oracle InForm, or similar EDC systems.Strong understanding of GCP, ICH, and clinical research processes.Excellent communication and leadership skills.What IQVIA Offers Fully remote role – company equipment providedCompetitive salary and performance-based incentivesCareer growth and learning opportunities through mentoring and internal mobilityInclusive, global culture focused on innovation and collaborationWhat to Expect After Applying Recruiter video chat (20 min)Hiring manager interview (1 hour, MS Teams - Offer decisions are typically made within one or two weeks of the final interview.)  Apply now to join IQVIA, where your expertise shapes the future of data-driven healthcare! IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

IQVIA is growing! Hiring multiple Clinical Data Management (CDM) Leads across our FSP (Functional Service Provider) and Traditional (Sponsor-Agnostic) delivery models. Apply now and have your resume considered for Lead Data Manager opportunities across multiple teams - allowing us to match you with the best-fit project and client environment for your experience and interests!  IQVIA is seeking experienced Clinical Data Management Leads to oversee end-to-end data management delivery for global clinical trials. You’ll ensure quality, accuracy, and compliance while leading cross-functional teams that help bring new therapies to life. This is a remote/WFH position with all necessary equipment provided.What You’ll Do Lead data management for complex, global clinical trials from study setup to database lock.Serve as the main client contact for all data management deliverables.Oversee SAE, PK, and external data reconciliation and database deployment.Manage timelines, budgets, and resource allocation to meet customer expectations.Mentor junior data management staff and promote best practices.Drive process improvements and ensure regulatory and SOP compliance.Who We’re Looking For Ideal candidates will have.... Bachelor’s degree in life sciences, health, clinical, biological, or mathematical field.No less than 10 years of direct clinical data management experience, with 5+ years in a Lead Clinical Data Management role.Your previous roles/job titles may include Clinical Data Manager, Senior Clinical Data Manager, Lead Data Manager, Principal Data Manager, and/or Data Management Project Manager.Proven success managing large global studies (1000+ patients).Expertise with Medidata Rave, Oracle InForm, or similar EDC systems.Strong understanding of GCP, ICH, and clinical research processes.Excellent communication and leadership skills.What IQVIA Offers Fully remote role – company equipment providedCompetitive salary and performance-based incentivesCareer growth and learning opportunities through mentoring and internal mobilityInclusive, global culture focused on innovation and collaborationWhat to Expect After Applying Recruiter video chat (20 min)Hiring manager interview (1 hour, MS Teams - Offer decisions are typically made within one or two weeks of the final interview.)  Apply now to join IQVIA, where your expertise shapes the future of data-driven healthcare! IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

About IQVIA: IQVIA is a fast-growing and highly successful business, delivering data-driven insights and measurable impact for clients across the global life sciences ecosystem. Leveraging access to some of the world’s most comprehensive healthcare data, advanced analytics and research capabilities, IQVIA experts design and deliver innovative, technology-enabled evidence programs to support decision-making across the product lifecycle. Job Description: We are looking for a highly motivated HTA Analyst-Programmer to support health technology assessment (AMNOG) and market access activities in Germany. The role is ideally suited for biostatisticians or data scientists with a strong interest in applying clinical evidence to reimbursement and market access decision-making. A substantial part of the role involves statistical programming. Key Responsibilities: Contribute to the development of German AMNOG dossiers, with a focus on programming of statistical analyses for Module 4 Perform scientific assessment and analysis of clinical trial data, including analysis of efficacy, safety, patient-relevant endpoints, and subgroup analyses Perform meta-analyses and indirect treatment comparisons and support interpretation of statistical outputs Contribute to the automation and standardization of analysis workflows to ensure efficiency, consistency, and reproducibility Collaborate closely with cross functional teams (Market Access, HEOR, Medical Affairs, EU-HTA Team) Ensure scientific quality, clarity, and consistency of generated outcomes Monitor and interpret methodological developments from IQWiG, G BA, and relevant HTA bodies Your Profile: Education & Technical Background Master’s degree or PhD in biostatistics, data science, or a related field Initial experience in HTA, AMNOG, HEOR, or Market Access (industry, consultancy, or research institute preferred) and/or in clinical development Solid understanding of clinical study designs, endpoints, and statistical principles Familiarity with clinical study data and the corresponding industry standards (CDISC SDTM/ADaM) Familiarity with the German AMNOG process, IQWiG methodology, or G‑BA procedures is an advantage Skills Strong analytical skills and attention to detail Ability to translate complex data into clear and structured output Affinity for data and excellent analytical and conceptual skills Strong background in statistics/data sciences/programming with a focus on process automation >2 years experience in advanced SAS programming, R programming skills are an advantage >2 years hands-on clinical data analysis experience with CDISC SDTM/ADaM datasets Solid understanding of core statistical methods used in clinical trials and HEOR Personal Competencies Structured, reliable, and quality‑driven working style Strong teamwork and communication skills Fluent German and English, written and spoken (this is an absolute must) Strong strategic and critical thinking skills focus on quality, service, and solutions. Well-organized, highly independent, highly motivated Strong customer orientation, a high level of responsibility and reliability High attention to detail, and audit-ready mindset Please submit your CV in English. IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com. IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. At IQVIA, we believe that diversity, inclusion, and belonging empower our mission to accelerate innovation for a healthier world. We create a culture of belonging by valuing the perspectives of all talented employees worldwide and providing them with the opportunity to power smarter healthcare for everyone, everywhere. When our talented employees bring their authentic selves and their diverse experiences to work, they enable us to accomplish extraordinary things. Multifaceted thought processes spark innovation. Multi-talented collaboration harnesses innovation to deliver superior outcomes. Likewise, as part of this culture, IQVIA is committed to ensuring effective equality between women and men, integrating it as a strategic principle in its corporate and human resources policies.

Required skills and experience:• 2/3+ years of experience working with Azure and/or AWS or any other major cloud platform technologies• Provisioning, operating, and maintaining systems running on Azure and AWS cloud platforms including deployment/teardown and automation• Proficient with cloud platforms including IaaS & PaaS components, for example: Azure Virtual Machines/EC2 Instances, Golden Image/AMI management, Storage Accounts/S3 buckets, Network Security Groups/Security Groups, vNets/VPCs, Azure App Services, AWS Lambda, Kubernetes etc• Infrastructure as code (IaC), and CI/CD pipeline experience is required – example: Terraform, Bicep/ARM, CloudFormation, Gitlab, ADO• Hands-on scripting and automation experience (e.g., PowerShell, Python, Bash, Azure CLI, AWS CLI)• Proficient understanding of Windows and Linux operating systems from an administration perspective including OS configuration, patching, performance tuning, user/group management, system services, and troubleshooting• Knowledge of network (LAN, WAN, VPN) and web related protocols (e.g. TCP/IP, UDP, IPSEC, HTTP, HTTPS, routing protocols)• Management of monitoring and metrics using Azure Monitor, Log Analytics, Application Insights, CloudWatch and shared dashboards• Configuration and operation of backup solutions to protect and recover workloads (Azure Backup, AWS Backup)• Update Management (patching) experience on cloud based systems is required including remediation of patching issues• Experience with security policies, RBAC models, IAM roles and access provisioning, Security Groups• Good awareness of the latest features/capabilities of Azure and AWS platforms are desirable• Knowledge on installation, configuration, usage of CLI tools to manage cloud components is desirable• Experience with creation and maintenance of operations documentation for day to day issues and knowledge transfer• Excellent troubleshooting skills for Azure/AWS platforms including OS-level issues• Experience with ITIL/ITSM service operations processes including incident/request management, change and configuration management. Ideally ITIL Foundation certified. ServiceNow exposure is a bonus• Good to have: Understanding of AI-driven operations (e.g., AIOps, AI-assisted troubleshooting, log analytics insights)• Prior experience in Life Sciences area is also a bonus. Other highly regulated industry experience will be considered alsoEducation/certification:•    Degree level educated, preferably in science, maths or engineering areas.•    Azure Certification is a must - preferably Azure Administrator or Solutions Architect certified. AWS Associate level certification is preferred. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Required skills and experience:• 1/2+ years of experience working with Azure or AWS or any other major cloud platform technologies• Provisioning, operating, and maintaining systems running on Azure or AWS including deployment/teardown and automation support• Understanding of cloud platforms including IaaS & PaaS components, for example: Azure Virtual Machines/EC2 Instances, Storage Accounts/S3 buckets, Network Security Groups, vNets, VPCs, Azure App Services/AWS Lambda, Kubernetes basics etc• Exposure to scripting or automation tools (e.g., PowerShell, Python, Bash, Azure CLI, AWS CLI) is desirable• Understanding of Infrastructure as code (IaC) and CI/CD pipeline concepts – example: Terraform, Gitlab, ADO• Good practical experience with Windows and Linux operating systems, including administration tasks such as OS configuration, patching, user management, system monitoring, and troubleshooting• Knowledge of network (LAN, WAN, VPN) and web related protocols (e.g. TCP/IP, UDP, HTTP, HTTPS)• Exposure to monitoring tools such as Azure Monitor, Log Analytics, Application Insights or AWS CloudWatch is desirable• Understanding of backup and patching concepts in cloud environments• Awareness of security concepts such as RBAC, IAM roles, access provisioning and secure configurations• Good awareness of cloud platform capabilities and willingness to learn new features• Knowledge on installation, configuration, usage of CLI tools to manage cloud components is desirable• Experience with documentation and following operational runbooks is desirable• Good troubleshooting and analytical skills for cloud issues• Understanding of ITIL/ITSM processes including incident/request management. ServiceNow exposure is a bonus• Good to have: Awareness of AI concepts and their applicability in IT operations (e.g., automation, monitoring insights)• Prior experience in Life Sciences area is also a bonus. Other highly regulated industry experience will be considered also Education/certification:•    Degree level educated, preferably in science, maths or engineering areas.•    Azure or AWS Fundamentals level certification is preferred. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Required skills and experience:• 2/3+ years of experience working with Azure and/or AWS or any other major cloud platform technologies• Provisioning, operating, and maintaining systems running on Azure and AWS cloud platforms including deployment/teardown and automation• Proficient with cloud platforms including IaaS & PaaS components, for example: Azure Virtual Machines/EC2 Instances, Golden Image/AMI management, Storage Accounts/S3 buckets, Network Security Groups/Security Groups, vNets/VPCs, Azure App Services, AWS Lambda, Kubernetes etc• Infrastructure as code (IaC), and CI/CD pipeline experience is required – example: Terraform, Bicep/ARM, CloudFormation, Gitlab, ADO• Hands-on scripting and automation experience (e.g., PowerShell, Python, Bash, Azure CLI, AWS CLI)• Proficient understanding of Windows and Linux operating systems from an administration perspective including OS configuration, patching, performance tuning, user/group management, system services, and troubleshooting• Knowledge of network (LAN, WAN, VPN) and web related protocols (e.g. TCP/IP, UDP, IPSEC, HTTP, HTTPS, routing protocols)• Management of monitoring and metrics using Azure Monitor, Log Analytics, Application Insights, CloudWatch and shared dashboards• Configuration and operation of backup solutions to protect and recover workloads (Azure Backup, AWS Backup)• Update Management (patching) experience on cloud based systems is required including remediation of patching issues• Experience with security policies, RBAC models, IAM roles and access provisioning, Security Groups• Good awareness of the latest features/capabilities of Azure and AWS platforms are desirable• Knowledge on installation, configuration, usage of CLI tools to manage cloud components is desirable• Experience with creation and maintenance of operations documentation for day to day issues and knowledge transfer• Excellent troubleshooting skills for Azure/AWS platforms including OS-level issues• Experience with ITIL/ITSM service operations processes including incident/request management, change and configuration management. Ideally ITIL Foundation certified. ServiceNow exposure is a bonus• Good to have: Understanding of AI-driven operations (e.g., AIOps, AI-assisted troubleshooting, log analytics insights)• Prior experience in Life Sciences area is also a bonus. Other highly regulated industry experience will be considered alsoEducation/certification:•    Degree level educated, preferably in science, maths or engineering areas.•    Azure Certification is a must - preferably Azure Administrator or Solutions Architect certified. AWS Associate level certification is preferred. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

IQVIA is growing! Hiring multiple Clinical Data Management (CDM) Leads across our FSP (Functional Service Provider) and Traditional (Sponsor-Agnostic) delivery models. Apply now and have your resume considered for Lead Data Manager opportunities across multiple teams - allowing us to match you with the best-fit project and client environment for your experience and interests!  IQVIA is seeking experienced Clinical Data Management Leads to oversee end-to-end data management delivery for global clinical trials. You’ll ensure quality, accuracy, and compliance while leading cross-functional teams that help bring new therapies to life. This is a remote/WFH position with all necessary equipment provided.What You’ll Do Lead data management for complex, global clinical trials from study setup to database lock.Serve as the main client contact for all data management deliverables.Oversee SAE, PK, and external data reconciliation and database deployment.Manage timelines, budgets, and resource allocation to meet customer expectations.Mentor junior data management staff and promote best practices.Drive process improvements and ensure regulatory and SOP compliance.Who We’re Looking For Ideal candidates will have.... Bachelor’s degree in life sciences, health, clinical, biological, or mathematical field.No less than 10 years of direct clinical data management experience, with 5+ years in a Lead Clinical Data Management role.Your previous roles/job titles may include Clinical Data Manager, Senior Clinical Data Manager, Lead Data Manager, Principal Data Manager, and/or Data Management Project Manager.Proven success managing large global studies (1000+ patients).Expertise with Medidata Rave, Oracle InForm, or similar EDC systems.Strong understanding of GCP, ICH, and clinical research processes.Excellent communication and leadership skills.What IQVIA Offers Fully remote role – company equipment providedCompetitive salary and performance-based incentivesCareer growth and learning opportunities through mentoring and internal mobilityInclusive, global culture focused on innovation and collaborationWhat to Expect After Applying Recruiter video chat (20 min)Hiring manager interview (1 hour, MS Teams - Offer decisions are typically made within one or two weeks of the final interview.)  Apply now to join IQVIA, where your expertise shapes the future of data-driven healthcare! IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Job OverviewUnder guidance, bridges and codes data into IQVIA systems. Essential Functions• Codes data, as required, transforming incoming paper data from suppliers to electronic data files.• Interprets written responses and enter into electronic coding systems allocating data to standard reference systems.• Performs quality assurance on coded data to ensure it accurately reflects the paper data submission.• Bridges data, comparing incoming transaction data with IQVIA’ reference data files to make a match or bridge between the two using manual or automated processes. Qualifications• High School Diploma or equivalent  Req• Three (3) years work experience in which PC literacy skills including Word, Excel have been gained. Req• Ability to carry out some analysis and information gathering to resolve problems on routine matters.• Developing knowledge of the company's products and pharmaceutical industry. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

所属部署・チーム名 Japan RBU 契約管理部※法人上の所属は「ソリューションズ（契約管理部）」となります。 部署概要 本部門は、ソリューションズおよびサービシーズのCSMSに関連する顧客契約およびベンダー契約を担当しています。両法人にまたがる契約書対応を行う専門チームであり、Japanローカル組織としてプレジデント直轄の位置づけにあります。 主要なステークホルダーは、営業部門、プロジェクトマネージャー、法務、財務、人事など多岐にわたります。 業務内容 クライアント、ベンダー、データ提供者、その他第三者との契約書・注文書等のドラフト作成およびレビュー相手方からの契約文書に対する修正要求の精査と受け入れ可否の判断契約成立までの受発注手続きのトラッキング各種登記に必要な書類の準備社内各部署からの弁護士・弁理士等への相談窓口として、社外（IQVIAグループ含む）専門家との連携その他契約書作成に関連する業務全般チームの特徴 設立から約1年の新しい組織であり、従来はソリューションズおよびサービシーズCSMSにそれぞれ契約管理部が存在していました。現在は業務効率と生産性の向上を目指し、属人的なノウハウを組織的な仕組みへと転換するフェーズにあります。 契約に関する幅広い知識の習得を重視し、法務とは異なる契約書専門性の追求にこだわりを持っています。また、日々の業務においては「凡事徹底」を掲げ、ルーティン業務の確実な遂行にも注力しています。 ポジションの魅力・キャリアパス ビジネスは契約によって成立しており、その種類や内容は多岐にわたります。契約書の条文一つで企業のリスクが大きく左右されるため、判断に伴う責任と権限は非常に重要であり、やりがいのある業務です。 部内では、派遣契約から業務委託契約、M&A関連業務まで幅広い契約に携わる機会があり、契約書の作成者から確認者へのステップアップも可能です。習得したスキルは長期的に活用できる専門性の高いものです。 応募要件 企業法務または契約関連業務における2年以上の実務経験ビジネスレベルの日本語（読み書き・会話）社内外ステークホルダーとの円滑なコミュニケーション能力Word、Excel、PowerPoint等の基本的な操作スキル歓迎要件 英文契約書の対応経験その他 繁忙期において月間30時間程度の残業が可能な方（1日あたり2〜3時間程度）期待される役割と成長ステップ 成長ステップ ・入社〜3ヶ月 サービスラインや申請フロー等、業務遂行に必要な基盤の習得 ・4〜12ヶ月 担当契約書のOJTを通じて、指導を受けながらも大半の業務を単独で遂行 ・13〜18ヶ月 イレギュラーな契約書を除き、単独での対応が可能に ・19〜24ヶ月 全ての契約書を単独で対応可能となり、契約書以外の周辺業務にも対応 IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Job Overview Associate Clinical Project Managers are an integral part of clinical trial delivery, liaising with clinical teams to improve patients’ lives by bringing new drugs to the market faster. The Associate Clinical Project Manager is a member of the core project team responsible for project delivery of clinical studies to meet contractual requirements in accordance with SOPs, policies and Company practices. Clinical Project Management is focused on project delivery, productivity and quality resulting in strong financial performance and customer satisfaction. The Associate Clinical Project Manager has distinct responsibilities supporting the efforts of the Clinical Project Manager to drive operational excellence and strategic leadership with our customers. Associate Clinical Project Managers may run their own studies as part of their development and/or manage the Project's Third-Party Vendors. Essential Functions• Provide input in to the development of integrated study management plans with the core project team and/or sub-team, within a client-dedicated team.• Accountable for assigned portion of clinical studies as per the contract while optimizing speed, quality and cost of delivery and ensuring consistent use of study tools and training materials and compliance with standard processes, policies and procedures.• Set objectives of project sub-team(s), according to agreed upon contract, strategy and approach, effectively communicate and assess performance.• Collaborate with other functional groups within the company where necessary to support milestone achievement and to manage study issues and obstacles.• Monitor progress against contract and prepare/present project and/or sub-team information proactively to internal stakeholders. Support the project leader to prepare/present project and/or sub-team information proactively to external stakeholders.• Identify risk (positive and negative) and contingencies and partner with project leader in problem solving and resolution efforts.• Achieve project quality by identifying quality risks and issues, responding to issues raised by project sub-team members and partner with project leader planning/implementing appropriate corrective and preventative action plans.• May serve as primary (for small projects) or back-up project contact with customer.• Lead the efforts of a project sub-team, responsible for managing cross-collaboration of the sub-team to support milestone achievement and to manage issues and obstacles.• Support the project leader in ensuring the financial success of the project.• Forecast and identify opportunities to accelerate activities to bring revenue forward in partnership with the senior project leader.• Identify changes in scope and partner with project leader to manage change control process as necessary.• Identify lessons learned and implement best practices.• May be assigned as the primary contact for vendors leading project vendor management and vendor management related activities as per project requirements Qualifications• Bachelor's Degree In life sciences or related field required• More than 1 year of Clinical lead, Clinical Trials Manager, Project Management experience preferred.• Knowledge of clinical trials - Knowledge of clinical trial conduct, and skill in applying applicable clinical research regulatory requirements i.e. ICH GCP and relevant local laws, regulations and guidelines, towards clinical trial conduct. Broad protocol knowledge, therapeutic knowledge desired.• Communication - Strong written and verbal communication skills including good command of English language. Strong presentation skills.• Problem solving - Strong problem solving skills.• Organisation - Planning, time management and prioritization skills. Ability to organize resources needed to accomplish tasks, set objectives and provide clear direction to others, experience planning activities in advance and taking account of possible changing circumstances.• Prioritisation - Ability to handle conflicting priorities.• Quality - Attention to detail and accuracy in work. Results-oriented approach to work towards delivery and output.• IT Skills - Good software and computer skills, including MS Office applications including but not limited to Microsoft Word, Excel and PowerPoint.• Finances - Good understanding of project financials.• IQVIA Core Competencies - Ability to demonstrate all IQVIA competencies (Client Focus, Collaboration, Communication, innovation, Ownership).• Available for Home-based 근무형태/장소 - 업무 형태 : 재택근무가 가능합니다. - 근무 장소 : IQVIA 잠실 오피스 (송파구 송파대로 558 월드타워빌딩 13층, 2/8호선 잠실역 도보 4분) 채용 전형 - 이력서 접수 > 서류전형/Pre-screening > 면접전형 > 최종합격 > 입사 - 지원 방법 : 영문 CV를 첨부하여 본 공고를 통해 지원 (이력서 양식 자율) - Pre-screening 전형 : 1) IQVIA의 Pre-screening은 후보자의 응답 편의성을 위해 온라인 스크리닝으로 진행됩니다. 제출된 이력서 검토 후, 경력상 적합한 후보자에 한해 안내 메일이 발송됩니다. 안내 메일을 받으신 후, 72시간 내에 편하신 시간에 언제든 응답하실 수 있습니다.2) 관련 안내 메일 및 가이드에 따라, 메일 수신 후 72시간 내에 제출 완료해주시기 바랍니다.- 면접은 화상 혹은 대면으로 진행되며, 지원자 가능 일시에 맞추어 조율됩니다. - 각 전형 결과는 합격/불합격 여부와 관계없이 모든 지원자에게 안내됩니다. - 국가등록장애인 및 국가보훈 대상자는 관련법에 의거하여 우대됩니다. - 지원서 내용이 사실과 다른 경우 합격이 취소될 수 있습니다. Life at IQVIA - 조직 내 다양한 Internal Career Development 의 기회 - Employee Assistance Program (직원 고민 상담 지원 프로그램, 가족 포함) - 사내 동호회, 팀워크샵, 팀빌딩, 연말파티 등 다양한 Activity 지원 - 다양한 경조 패키지 (경조금/경조휴가/상조용품), 호텔 프로모션/리조트 멤버십 지원 - 명절상여금, 영유아 위탁교육비, 업무용 휴대폰(iphone) 지급 - 재택근무 활성화 및 모바일 오피스, Flexible working hours 운영 - 단체보험 (생명/상해보험, 배우자/자녀 포함) 및 건강검진 패키지 지원 - 연차 외 특별휴가 (Company day, 유급병가) 등 - 직원 추천 보너스 제도 추천 영상1. What does it mean to be IQVIAN? https://youtu.be/dhrtkSGsej4 2. 아이큐비아ㅣ나만 몰랐던 (진짜) 포브스 선정 '세계 최고의 직장' https://youtu.be/i8hNY49LzPs?si=Zzp2IoY4cqsD2x_e 관련 문의 한국 아이큐비아 채용(IQVIA) 카카오톡 채널을 통해 1:1 문의 하실 수 있습니다. http://pf.kakao.com/_XeVFs *채널을 추가하시면 매월 신규 포지션 알림 및 회사 소식을 받아보실 수 있습니다. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Job PurposeThe Regional Key Account Manager (SPOT Manager) plays a critical role in driving sustainable business growth, strategic customer development, and commercial excellence across the animal health market within the MENA region. Acting as the primary commercial leader for assigned markets, this role translates the client’s regional strategy into actionable business plans, accelerates sales performance, and ensures consistent brand execution while maximizing customer value and profitability. Operating within the International Division, the Regional KAM (SPOT Manager) serves as the key interface between the client, distributors/importers, and local market stakeholders across Egypt, KSA, Iraq, Jordan, Kuwait, Lebanon, Libya, and Yemen—ensuring alignment with business objectives, governance standards, and growth ambitions. Key Responsibilities1. Strategic PlanningDevelop and execute strategic plans for targeted markets to achieve and exceed sales targetsOwn and drive Business and Marketing plans across the assigned regionLead project creation across all phases (preparation, negotiation, and implementation)Drive market growth, deployment, and strategy for Royal Canin across MENA marketsProvide insights into market context, risks, and opportunitiesRecommend and develop locally relevant strategies2. Sales Performance & Market ExpansionEnsure accountability and delivery of annual sales targetsManage existing country scope effectivelyIdentify and drive opportunities to expand the client’s brand footprint3. Sales AccelerationDevelop and implement sales acceleration strategiesLeverage appropriate tools and solutions to enhance commercial performanceTrain and upskill importers’ sales teamsMonitor, measure, and optimize resultsManage P&L performance across marketsCoordinate business activities, priorities, and execution with importers4. Team LeadershipBuild, lead, and develop a high-performing teamOversee recruitment, onboarding, and team structureDefine team purpose, priorities, and ways of workingDrive performance, engagement, and development discussions5. Commercial ExcellenceExecute structured selling processes and drive sell-through performanceSupport importers in maintaining strong brand presence (scientific communication, merchandising, digital/online media guidelines)Conduct market analysis and report insights to Hub LeadershipCoach, motivate, and manage key customersEnsure accurate and timely reporting and administration6. Cross-Functional CollaborationWork closely with internal functions (Regulatory, Demand, Logistics, Corporate) to deliver annual plansPartner with Customer Service, Demand Planning, and Operations for smooth product flow and order executionCo-create ways of working (WoW) with importers and generate actionable insightsCollaborate with local sales teams to share best practices and market intelligence7. Governance & ComplianceEnsure compliant contracts between client and importers are signed on timeMaintain regular follow-ups in line with audit guidelinesSafeguard brand governance and alignment with global brand strategyQualifications & ExperienceEducation & Professional BackgroundBachelor’s degree in Business Administration or related fieldFluent in English; Arabic is mandatorySkills & CompetenciesStrong leadership and interpersonal skills with ability to influence across all levelsHigh energy, proactive, and results-oriented mindsetExcellent written and verbal communication skillsStrong organizational and stakeholder management capabilitiesAbility to make sound decisions with minimal supervisionStrong analytical skills with ability to identify issues and implement solutionsSelf-driven, innovative, and able to operate efficiently in a fast-paced environmentExperienceProven experience in Customer Management, Distributor Management, or Key Account ManagementExperience building and leading teams is a plusStrong proficiency in Microsoft Office (PowerPoint, Word, Excel)FMCG or animal health industry background is preferredExperience working in complex, fast-changing environmentsStrong project management and business development mindsetIQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Job OverviewPerform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. Essential Functions Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability. Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues. Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate. Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase. Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements. Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation. Collaborate and liaise with study team members for project execution support as appropriate. If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis. If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement. Qualifications Bachelor's Degree in scientific discipline or health care. Requires at least 1 year of on-site monitoring experience. Equivalent combination of education, training and experience may be accepted in lieu of degree. Good knowledge of, and skill in applying, applicable clinical research regulatory requirements (i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines). Good therapeutic and protocol knowledge as provided in company training. Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer and iPhone and iPad (where applicable). Written and verbal communication skills including good command of English language. Organizational and problem-solving skills. Effective time and financial management skills. Ability to establish and maintain effective working relationships with coworkers, managers, and clients. Candidates will be assessed according to their years of experience and be considered for various levels where applicable. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Clinical Pharmacist Type: Full-time, hybrid We are looking for pharmacists to join the team to work across Yorkshire. Join us in this exciting role where you will utilise your clinical expertise and commercial acumen to support patients with chronic conditions in primary care settings. As a clinical pharmacist at Interface Clinical Services, an IQVIA business, your responsibilities will include aiding practices with clinical tools, identifying opportunities for clinical reviews, ensuring adherence to protocols, and fostering awareness of Interface Clinical Services within primary care settings. This is the perfect role for a pharmacist who is looking for career progression! Some principal responsibilities: Support Practices to provide clinical tools and resource to help manage patients with long-term conditions. To ensure clinical services are delivered within the bounds of our protocols, service operating instructions and systems. To identify opportunities for clinical reviews at individual practice level, PCN or CCG level where there is clinical need. To enhance the awareness of Interface Clinical Services within primary care and to assist in developing long lasting relationships with practices and local NHS organisations. Ideal candidate: Must be a GPhC registered pharmacist. MPharm essential. CPPE / PCPEP desirable. Community or primary care experience desirable. Willing to travel as required, along with remote (home) working. A keen passion to make a positive difference to patients’ long-term health. Driven work ethic. Benefits of working as Clinical Pharmacists with IQVIA: Funding and paid leave for the Independent Pharmacist Qualification. Access to learning and career path development tools. Become a clinical expert in long term conditions eg AF, asthma, COPD, diabetes, heart failure. Car allowance £5500 (PLUS paid mileage). 25 days annual paid holiday, NO weekend, bank holiday or evening working. Opportunity to buy extra 5 days annual leave. Competitive open-ended bonus. Private healthcare (BUPA). Flexible benefits including private dental, competitive pension scheme, Life Assurance, Group Income Protection, Personal Accident Insurance and more! Online wellbeing support available 24 hours a day, 7 days a week, 365 days a year. Other benefits at corporate rates such as: gym memberships, access to 100s of restaurant/store discounts. Regular remote coffee mornings, regional meetings / team social events. Manage your own diary to enable flexible working and in practice. Be part of the team and apply today! Interface Clinical Services, an IQVIA business, are the largest organisation within the UK healthcare sector to fully employ a team of pharmacists. We operate in partnership with both the NHS and industry. As pioneers of Clinical Pharmacist-led services, here at Interface we believe that a career in healthcare is more than just a job, it’s a vocation. Our mission is simple, to improve clinical outcomes and improve patients’ lives, we want you to be part of that journey and know that you are making a difference. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Position Title: Mobile Nurse (LPN/LVN) – Per Diem, In-Home Services    Location: Various U.S. locations (local travel within designated geographic area)    About the Role: IQVIA’s In-Home Clinical Solutions team seeks a qualified and dedicated Mobile Licensed Practical Nurse (LPN) or Licensed Vocational Nurse (LVN) to deliver in-home clinical services to patients initiating therapy with complex medications. This per diem role involves traveling to patient residences to perform clinical services such as, but not limited to, phlebotomy, electrocardiograms (EKGs), and macular edema screenings in support of treatment initiation and adherence strategies.    This is a per diem, travel-based role offering flexible hours, with no minimum monthly visit requirement. Referrals are assigned based on your geographic availability and program demand. IQVIA manages all scheduling and patient communication, allowing you to focus entirely on clinical care.     Position Details:  Per diem, mobile-based role with flexible scheduling  No minimum monthly visit commitment required  Paid hourly compensation that includes the appointment time and travel time to/from patient’s home. (2 hour minimum paid)  IRS-standard mileage rate reimbursement.    Key Responsibilities:  Perform in-home blood specimen collection, labeling, and transporting specimens according to network policies, procedures, and regulatory standards.  Comply with all laboratory safety and handling procedures; ensure appropriate delivery to designated laboratories.  Conduct screenings as has been appropriately trained to conduct, including but not limited to electrocardiograms (EKGs) and macular edema screening exams (training provided).  Maintain a clean and organized work environment, including transportation and supplies storage specific to the In-Home Network.  Monitor and manage clinical supply inventory.  Collaborate with IQVIA’s clinical coordination team to execute and submit appropriate visit-related paperwork promptly and accurately.   Identify and report adverse events, medical product complaints, or patient inquiries in accordance with IQVIA and manufacturer guidance.  Maintain accurate mileage and time logs for reimbursement and compliance purposes.    Qualifications:  Active and unrestricted LPN or LVN license required  Current CPR certification required  Minimum 2 years of phlebotomy experience in clinical or field settings required  At least 1 year of EKG experience preferred  Certification as a Certified Medical Assistant (CMA) or Phlebotomy Technician (CPT) preferred.  Ability to lift up to 70 pounds to transport medical or diagnostic equipment (e.g., eye exam kits).  Ability and willingness to travel up to 100 miles to conduct patient visits.  Proficiency in using medical equipment and upholding proper documentation practices.  Strong interpersonal and communication skills with a patient-focused approach.  Fluent in spoken and written English.  Must possess a valid driver’s license and will be subject to a review of driving record prior to hire.  Must complete a drug screening and background check after accepting an offer.    #LI-CES  #LI-DNP  IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. The potential base pay range for this role is 28.00 per hour. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.