IQVIA

Essential Duties & Responsibilities Collaborate as an integral part of the client Core Team which comprises of meeting planners and speaker bureau planners and other planner roles supporting the logistics of each meeting.Coordinate all aspects of the planning and delivery of relevant meeting logistics in a timely manner within the client’s business rules and budgetary requirement.Confirm and secure location/venue booking of each meeting assigned, applying venue compliance following business rules and approved SOP of each client team.Plan and confirm Food & Beverage needs of the meeting for the Sales Rep, Speaker and all attendees considering any requested special F&B needs of the meeting.Review and secure all audio-visual needs for the meeting including specific requests or needs by the Sales Rep or the Speaker(s) of the meeting.Coordinate venue, food/beverage, and AV confirmation with Meeting Planner through standard documentation and communication within the meeting lifecycle.Ensure all related tasks, required documents are sent and confirmed in a timely manner as measured by task due dates and applicable service level deliverables.Communicate timely with meeting planner, speaker bureau planner and vendors related to task completion and other related inquiry or follow up needs.Application of client business and compliance rules throughout the planning process, especially related to venue appropriateness and negotiated rates within compliance rules.Ability to trigger or escalate any items that can impact risk on meeting compliance.Complete work within client defined SLA parametersEnsure understanding of system functionalities related to job function as assigned.Liaise with relevant internal and external stakeholders to ensure appropriate team members have the most up to date information.Comply with timekeeping standards & policies in Sprout, PSA ensuring accurate work hours are logged.Qualifications 2+ years of (events) planning, and/or customer service experience or equivalentPrevious work experience in catering to US clients, preferably in a phone-based Customer Service role, is requiredRelevant events or meeting planning experience is preferredPharma Industry experience is a plusFamiliarity with US cultural norms and practices to better understand and service stakeholders and clients.Bachelor's Degree Required.Proficiency in PC applications, Microsoft Office suite of products (Word, Excel, PowerPoint, Teams) and Outlook is required.Knowledge in SharePoint, Salesforce and Smartsheet preferred.Proficiency in using phone systems such as Twilio, CRM software and other relevant technology is preferredAbility to carry out analysis and information gathering to resolve problems on routine matters.Able to work during US standard business hours and be flexible on work schedule and/or extended hours to meet clients’ business needs during peak season.Ability to multi-task/plan numerous meetings simultaneously while still demonstrating a strong attention to detail.Able to be flexible to report onsite frequently, dependent on business needConducive work space when working remotely at home, which includes ability to receive and make calls during your shift, work with company provided dual monitors and have appropriate internet speed is requiredComfortable working in a fast-paced team environment, while also able to work independently.Exceptional customer service skillsA strong sense of urgency and the ability to effectively problem solve.Excellent oral and written communication skills with focus on the ability to be concise and clear, summarize a situation and articulate the necessary next steps, effectively listen, and assess the need for urgent action.Collaborate as an integral part of the project team to execute world class events as measured by internal and external client satisfactionWilling to work in graveyard shiftAmenable to work in Mckinley TaguigIQVIA 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, controls the report generation process and provides guidance and support to clients daily or as a specialist on specific products/services.Essential Functions Ensures the contract fulfillment to specifications of basic and routine reports for defined customers.Reviews client data requirements with the appropriate internal resource to ensure that basic product deliverables meet the customer's specifications, including timeliness and quality.Follows IQVIA data verification protocols.Researches, analyzes and responds to client inquiries that are routine in nature.Provides support to team for client service meetings at customer sites.May produce ad-hoc studies on demand.Job Qualifications Bachelor's Degree requiredTwo (2) years related work experienceExperience in an IQVIA role preferred and pharmaceutical experienceProficient in PC applications such as ExcelAbility to communicate effectively with various levels in the organization (written and oral)Demonstrate problem solving, analytical and strong customer service skillsIQVIA 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 supervision, provide support enabling the accurate and timely payment administration to our network of project sites.  Perform duties in accordance with IQVIA Finance Standard Operating Procedures (SOPs), Sarbanes-Oxley Controls and Unit Service Level agreements (if applicable).  Essential Functions Managing a portfolio of projects and providing oversight on the entire process. Ability to form remote relationships with colleagues across the globe, consider indirect influences on your work and manage these.Highlighting aged invoices and financial risks – give reasons why for any delaysData quality control, ensuring batches are scheduled as per contracts and meeting the budgetsProject reconciliationsPayment cycle target trending – ensuring the studies are meeting the target for each step in the payment cycleProviding high level of customer service to internal project teams and assisting them in any project related issues by finding resolution. Ability to influence others and ensure that key actions are takenTrack and report metric data flagging nonstandard issues to project teams / line managerProvide assistance to other team members as required, to ensure the group meets targets.Check that appropriate approvals are obtained for set up and payment process.Provide support and participate in teams handling various routine tasks.Provide standard reports and run KPI for the project teamsPerform other duties as assigned.File appropriate documents.QualificationsHigh School Diploma or equivalentPrevious experience in systems would be an advantage however full training will be provided 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 OverviewSupport the delivery of all required start-up contracting activities for selected sponsors, studies or multi-protocol programs as determined by either the agreed algorithm or the Sponsor’s requirements, including pre-award activities. Essential Functions• Develop simple investigator grant estimates and proposal text to support the proposal development process.• Utilize and maintain contract and budget templates and contracting systems, tools, processes, and training materials for selected sponsors, studies or multi-protocol programs according to the Scope of Work and Project Plan, within the agreed project strategy.• Ensure collaboration, including communication with sponsors, stakeholders and RSU regions and countries, to successfully deliver the agreed project scope in compliance with sponsor requirements and/or the RSU Management Plan.• Provide specialist operational and financial contracting support to facilitate efficient business development and initiation and maintenance of clinical trials, whilst enabling compliance with regulatory requirements.• Assist in the creation and/or review of core scientific, technical and administrative documentation to support business development and enable study initiation and maintenance, as required.• Contribute to the collection, interpretation, analysis and dissemination of accurate contracting intelligence to support assigned studies and the wider company, as required.• Ensure overall contracting efficiency and adherence to project timelines and financial goals; report contracting performance metrics and out of scope contracting activities as required.• Comply with contract management and quality standards. Provide administrative and operational support to investigator site contract analysts, managers and directors as required.• Ensure accurate completion and maintenance of internal systems (with emphasis on CTMS), databases, tracking tools, timelines and project plans. Qualifications• Bachelor's Degree• Required at least 1 year of site contracting relevant experience.• Coordinate the development of investigator grants and estimates, contracting strategies and proposal text to support the proposal development process.• Life sciences or medically related field including biopharmacuitical's clinical research experience.• Finance administration, accounting (Manages and process payments related to all clinical trials contracts in the financial and payment) 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.

Graphic Designer – Life Sciences Role Overview We are seeking a creative and detail-oriented Graphic Designer to design and develop high-quality digital and print assets for global life sciences/pharmaceutical clients. The role requires strong visual storytelling skills and hands-on expertise across Adobe and video design tools. Key Responsibilities Creative Design & Asset Development Design digital assets: banners, emailers, infographics, visual aids, and social creativesDevelop multimedia content: 2D/3D videos, animations, and motion graphicsCreate print assets: brochures, leave-behinds, magazines, and promotional materialsTranslate brief requirements into visually compelling, brand-compliant designsLife Sciences Content Adaptation Work with medical, marketing, and content teams to convert complex scientific content into easy-to-understand visual formatsEnsure all creatives adhere to brand guidelines and compliance standards (MLR awareness preferred)Stakeholder Collaboration Liaise with internal teams and client stakeholders to understand requirements, iterate designs, and deliver on timelinesIncorporate feedback effectively while maintaining design quality and consistencyProduction & Quality Control Prepare final files for digital publishing and print productionEnsure accuracy, consistency, and high-quality output across formatsRequired Skills & Experience 2–4 years of experience in graphic design (agency or healthcare/life sciences preferred)Strong portfolio demonstrating digital + print + video design workTools Expertise: Adobe Creative Suite:Photoshop, Illustrator, InDesign (mandatory)Video/Motion tools (any of):After Effects, Premiere Pro, Blender, or similar toolsDesign Capabilities: Strong understanding of layout, typography, color theory, and brandingExperience in infographics, visual storytelling, and multimedia designWorking knowledge of 2D/3D design and animation conceptsPreferred Qualifications Experience working with pharmaceutical / healthcare clientsFamiliarity with MLR processes and regulated content environmentsBasic understanding of UX/UI principles for digital formatsKey Traits High attention to detail and accuracyAbility to manage multiple projects under tight timelinesStrong communication and stakeholder management skillsCreative thinker with a problem-solving 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.

FSP Senior Epidemiologist (Oncology) Core Function Description: Design and conduct epidemiological studies to generate real-world evidence within time, budget, and quality standards, including but not limited to natural history of disease, population characterization, assessment of treatment patterns and unmet need, development of external comparators, benchmarking of clinical outcomes, comparative safety and effectiveness research, and post-authorization studies. Skill sets of the Epidemiologist role are similarly required, with the expectation of more experience, able to operate strategically under limited supervision, well versed in current Epidemiology research methods, deep understanding of how RWE fits within drug development, regulatory, medical, safety and other functions. Required Experience Lead development of study protocols, analysis plans, and study reports to answer research questions of priority to RWE.Lead, design, and manage epidemiological, biomarker and/or data science projects.Lead, plan, design, and conduct analyses for internal and external decision making (e.g., responses to regulatory authorities, rapid analyses of safety queries).Lead the identification of fit-for-purpose data for the timely execution of the RWE strategy.Constructed cohorts using RWD sources (e.g., claims, EHR) and evaluate key variables, including diagnosis and procedures codes, and plan validation studies as needed.Contribute to the communication of observational research results and methods, including development of pertinent sections of regulatory documents, reports, publications, white papers.Support the effective communication of study/analysis results to support internal and external decisions.Coauthor abstracts and manuscripts for external dissemination of methodologic study results.Contribute to the development of processes and training aimed at increasing the efficiency, quality, and impact of functional activities.• Technical Expertise: Observational research methods (both Primary and Secondary), deep knowledge of biostatistics and analysis methods, understanding of regulatory processes.Ability to design studies independently, (i.e., ability to translate research questions to create study design).• Subject Matter Expertise: Extensive experience conducting cancer epidemiology studies (solid tumor experience a plus), experience with commercial Oncology EMR databases.Leverage RWE expertise to identify evidence gaps and develop options to address the evidence gaps in support of Clinical Development Programs in early phase (ph1/2).Provide subject matter expertise and conduct analyses for descriptive and comparative research using RWD (examples include claims, EHR, registry data) for methodologic research questions.Expert knowledge and extensive experience with cancer epi (solid tumor experience a plus), extensive experience with oncology EMR databases, extensive experience with conducting cancer epi studies.Experience with Clinico-genomic multi-modal data (e.g., Tempus AI) or population biobank data (UK biobank) is a plusMinimum Qualifications PhD in Epidemiology, Biostatistics, Psychometrics, or related field with a minimum of four (4) years of relevant post-doctoral experience, preferably in pharmaceutical industry, biotechnology, or consulting environment. Master’s degree in epidemiology, biostatistics, bioinformatics, or relevant scientific field, plus 7-9 years of experience in lieu of PhD may be acceptable.Deep understanding of observational research methods and experience to support the design and conduct of observational research, including protocol, statistical analysis plan, and study report development.Extensive knowledge of secondary data sources and experience with secondary data analysis, including electronic medical record and/or medical claims databases.A record of scientific publications demonstrating expertise in observational study design, analysis, and interpretation is preferred.Demonstrated ability to function with an increasing level of autonomy and to develop productive cross- functional collaborations in a matrix environment.Ability to manage priorities and performance targets.Experience in leading drug development project for 2+ years for therapeutic area of assignment 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 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 $125,800.00 - $350,300.00. 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.

The Senior Clinical Trials Assistant will play a vital role in supporting Local Trial Managers and Clinical Research Associates across global trials. Key deliverables include tracking progress of the clinical trial, managing study data, budget, investigational products, mailings and correspondence and other relevant tasks in support of the Local Trial Managers and Clinical Research Associates. We are seeking candidates with previous CTA experience supporting global trials. Key Responsibilities: Maintain and update clinical systems and documentation, including the Trial Master File.Support the preparation, distribution, filing, and archiving of clinical documents and reports.Conduct periodic reviews of study files to ensure completeness and compliance.Assist with clinical trial supply logistics and tracking.Manage Case Report Forms (CRFs), queries, and clinical data flow.Serve as a central point of contact for project communications and documentation.What We’re Looking For: Degree in life sciences or equivalent industry experience.Previous CTA experience, supporting global trials.Familiarity with Good Clinical Practice (GCP) and ICH guidelines.Proficiency in Microsoft Word, Excel, and PowerPoint.Strong written and verbal communication skills in English.Excellent time management, organization, and collaboration skills.Please note: This role is not eligible for UK visa sponsorship. 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.

Location: Oeiras (Lisbon ) - Hybrid Contract: Full-time Language Requirement: CV in English Join Us on Our Journey to Reimagine Healthcare IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services for the life sciences industry. With 85,000 employees across more than 100 countries, we create intelligent connections across the healthcare ecosystem through data, transformative technology, and deep industry expertise. We are now looking for a Key Account Manager to join our Sales team and support pharmaceutical clients in their growth strategies by leveraging IQVIA’s data assets and services. Role Summary: As a Key Account Manager, you will build and nurture client relationships, drive revenue growth, and identify new business opportunities across your assigned accounts. You will be the primary point of contact for strategic clients, ensuring they maximize the value of IQVIA’s solutions. Key Responsibilities: Client Engagement & Business Understanding Build, strengthen, and expand relationships across client organizations.Promote IQVIA products and services to achieve revenue targets.Develop a deep understanding of client priorities and translate them into actionable business opportunities.Create and execute strategic account plans.Act as a trusted advisor on marketing, market research, sales management, industry trends, and IQVIA capabilities.Commercial & Operational Excellence Manage contract renewals, subscriptions, and commercial performance metrics.Oversee internal and external financial processes (rebates, invoicing, accounts receivable, DSO).Maintain visibility on pipeline, recent wins, and strategic opportunities (keeping CRM systems updated with opportunities, activities, and account plans).Ensure high levels of client satisfaction in partnership with Client Service teams.Strategic Client Development Shape client perception by sharing relevant marketing materials and thought leadership.Facilitate peer-to-peer engagement by connecting clients with relevant IQVIA experts.Identify innovation opportunities aligned with client priorities and IQVIA’s strategic direction.Contribute to the broader Sales & Account Management community by sharing insights and best practices.Skills, Experience & Qualifications Minimum 2-3 years of experience in Sales, Consulting and/or Business Development within similar organizationsPrevious experience in pharma/healthcare sector will be considered a plusStrong interpersonal skills and ability to build long-term business relationships.Proven negotiation and influencing capabilities.Demonstrated proactivity and ability to identify and convert opportunities.Solid understanding of the pharma business model and life sciences commercial strategy.Experience working successfully in a matrixed organization.Excellent customer service mindset and ability to translate client needs into solutions.Strong judgment and decision-making skills.Minimum Bachelor degree in Engineering, Business Management, Pharmacy or related field.Fluency in English and PortugueseWhy Join IQVIA? At IQVIA, you can shape your career and choose the path that best supports your growth. With exposure to diverse geographies, capabilities, and therapeutic areas, you’ll find endless opportunities to learn, evolve, and make an impact. We believe that meaningful results come from the right people working in the right environment. Here, you’ll help clients drive healthcare forward and ultimately improve human health outcomes. It’s an exciting time to join us — and to reimagine what’s possible in healthcare. Moving healthcare forward. Together. IQVIA is committed to fostering a diverse and inclusive workplace. We believe that embracing diversity strengthens our teams, enhances innovation, and enables every employee to reach their full potential. 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.

IQVIA™ is The Human Data Science Company™, combining data, technology, advanced analytics, and human expertise to help healthcare clients improve outcomes for patients. Our solutions support better decision-making across the healthcare ecosystem and drive meaningful progress in life sciences. 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 to deliver scale, 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. Advisory Services Advisory Services is IQVIA’s global consulting engine and a leading advisor to life sciences and healthcare clients. We support global and regional headquarters across the full product lifecycle, addressing complex commercial and access challenges. Our work spans brand and go-to-market strategy, pricing and market access, portfolio and asset strategy, launch excellence, commercial model design, digital health optimization, and omnichannel engagement. We are a highly international team with a truly global way of working. Our culture emphasizes collaboration, analytical rigor, continuous learning, and practical impact. We leverage modern tools, standardized ways of working, and increasing use of automation and AI so our teams can focus on delivering meaningful outcomes for clients. Joining Advisory Services offers a rewarding career in life sciences consulting, with exposure to diverse therapy areas, geographies, and business challenges. Team members collaborate with leading experts in pharma and healthcare, benefit from continuous learning, and contribute to innovative thinking shaping the future of healthcare. We are currently looking for talented and passionate applicants at Analyst level to join the Global  Advisory Services Analytics & Consulting team with contract location in Oeiras, Portugal. Analysts in the Global  Advisory Services Analytics & Consulting Team play a critical role in the success of our projects and work in collaborative teams not only within Advisory Services but also with teams across geographies and functional areas. We expect our analysts to learn and gain expertise, to contribute to solutions and generate insights for our HQ clients in the healthcare and life science industry. Due to the importance of this role, we are looking for strong candidates who are highly data driven and apply their analytical and conceptual skills in generating actionable and strategic insights and recommendations for our clients. By joining the Global  Advisory Services Analytics & Consulting Team in Portugal, you will have the opportunity to work under the direct report of the Global IQVIA Advisory Services, supporting HQ clients around the world. Main Responsibilities: As an Analyst, you will be actively participating in the development, delivery, and management of Analytics & Consulting projects: Actively providing operational and strategic support throughout multiple client engagements with a strong focus on Commercial Effectiveness topics and Market & Therapy Assessment for international life science markets Handling IQVIA data assets, processing, designing and conducting analyses by using internal and external data to facilitate its understanding and interpretation in an insightful way for our clients Understand and communicate the “story behind the numbers”: together with the team, you will draw compelling insights to support our clients Assisting in data preparation, delivering components of the project with project management support and ensuring high quality of the final deliverable Developing broad knowledge of related consulting methodologies and of pharmaceutical and life science market through the delivery of consulting engagements, and participation in formal and informal learning opportunities Supporting the project team in developing and holding client presentations and workshops Contributing to internal initiatives and helping drive development of new services and product offerings Working willingly, proactively and effectively with the Global Advisory Services CSEC team and across the organization, to accomplish team’s goals and priorities by excelling in exploiting the remote-working model in its full potential  Qualifications, Experience and Skills: Bachelor’s or Master’s degree with a strong academic track record in engineering, economics or business administration, and life sciences related programs Enthusiasm and interest in key developments in healthcare industry through prior internship, project work, and/or work experience with max. up to 2 years Strong business acumen and understanding of sales & marketing business principals Demonstrate strong analytical, interpretative and problem-solving skills, working with large and multiple data sets to process data using different tools and formats Highly effective communication and remote working skills Strong capability in managing priorities so that deadlines are met while retaining consistent, high quality outcomes Ability to think creatively and strategically also under stressful situations Adaptability and ability to learn quickly and apply new knowledge Fluent written and spoken English is required.    We know that meaningful results require not only the right approach but also the right people. Regardless of your role, we invite you to reimagine healthcare with us. You will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve human health outcomes. Whatever your career goals, we are here to ensure you get there! We invite you to join IQVIA™. Please apply online with the usual personal information (cover letter, resume, references). 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.

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 IQVIA Laboratories 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, Python 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 Qualifications High School Diploma or equivalent 2+ years of relevant work experience or equivalent combination of education, training and experience. Self-driven. Keen attention to detail to anticipate, address and/or escalate issues, with aptitude to embrace and be conduit for change. Analytical 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. Computer proficiency including word processing, spreadsheet and Power Point applications. General understanding of medical, clinical research. 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 Medical Assistant / Phlebotomist – 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 Medical Assistant / Phlebotomist to support patient care by delivering in-home diagnostic services. 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:  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.  If located in the state of Washington or Louisiana, a state issued CMA or CPT license is required.  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 25.00 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.

IQVIA, fort de ses 88 000 collaborateurs à travers le monde, et fruit de la fusion entre IMS et QUINTILES, est le leader mondial du recueil, du traitement et de l’analyse des données de Santé. En France, IQVIA (environ 2000 salariés) dispose de nombreuses données sur les professionnels de santé (accessibilité à la visite médicale, appétence digitale, etc.) ainsi que de nombreux panels de médecins et pharmaciens au travers desquels nous produisons et vendons des rapports syndiqués, analysons la promotion et la communication des laboratoires pharmaceutiques et fournissons des recommandations sur les stratégies multi canal en cours et à venir. Missions : Au sein du Département des Ressources Humaines basé à La Défense, vous êtes rattaché(e) au Responsable des Relations Sociales et l'assistez sur l'ensemble des thématiques liées au droit du travail pour les différentes sociétés du périmètre France (6 entités légales) : Relations individuelles : Conseils et recherches juridiques permettant de répondre aux problématiques soumises par les opérationnels RH.Suivi des dossiers pré‑contentieux et contentieux de l'entreprise (rédaction de sanctions disciplinaires, lettres de convocation à entretien préalable et de licenciement, suivi des dossiers contentieux en collaboration avec les avocats, calcul des indemnités de licenciement…).Participer à la sécurisation de l'ensemble des processus juridiques et sociaux, à la rédaction et à la validation des documents juridiques internes.Préparer et animer des ateliers RH/juridiques auprès des managers opérationnels (recherches, préparation des supports, présentations). Rédiger des notes d'information internes sur des thématiques juridiques rencontrées par les opérationnels.Assurer une veille juridique et sociale (actualité légale, jurisprudence).Relations collectives : Participation à la mise en place d'accords collectifs (recherches juridiques, contribution à la rédaction de l'accord…).Contribuer à l’organisation des futures élections professionnelles.Aide à la préparation des réunions avec les IRP (CSE, CSSCT, commissions diverses…).Mettre à jour la Base de Données Économique et Sociale.Projets d’acquisition (Due Diligence) : Participer aux travaux de due diligence sociale dans le cadre des projets d’acquisition : analyse des contrats de travail, usages, accords collectifs, politiques RH, conformité sociale, risques juridiques potentiels.Identifier les écarts de conformité entre les pratiques de l’entité cible et celles du groupe, et contribuer à l’évaluation des risques (contentieux, coûts sociaux, obligations légales).Rédiger des notes de synthèse et recommandations à destination de la Direction, en lien avec les équipes Finance, Juridique et M&A.Contribuer à la sécurisation juridique des opérations de transfert (application du droit du travail, obligations d’information/consultation, impacts sur les contrats et avantages sociaux).Intégration post‑acquisition : Accompagner la mise en œuvre des obligations légales liées au transfert des salariés (information/consultation des IRP, communication interne, harmonisation documentaire).Participer à l’harmonisation des pratiques RH : contrats de travail, politiques internes, avantages sociaux, procédures disciplinaires, organisation du temps de travail.Contribuer à la gestion des impacts sociaux (changements organisationnels, évolutions de postes, alignement des statuts et classifications).Assurer un support juridique opérationnel aux équipes RH locales et aux managers durant toute la phase d’intégration.Suivre les actions post‑closing et contribuer à la sécurisation des processus RH dans le cadre de l’intégration dans le groupe.Profil : Formation : Issu(e) d'une formation juridique, vous préparez un diplôme de niveau Master 2, spécialisation en droit social, droit du travail ou relations socialesType de contrat : Alternance et apprentissage / possibilité au terme de la prise de poste de télétravailler, 2 jours par semaineConnaissances/compétences requises : Solides connaissances juridiques dans le domaine du droit social.Rigoureux(se), organisée(e) et autonome.Qualités rédactionnelles et de communication.Faculté à travailler en équipe et en transverse.Prise d'initiative.Bonne maîtrise du Pack Office.Localisation : Tour D2, 17 bis place des Reflets, 92400 Courbevoie, Esplanade de la Défense 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.

Medical Sales Representative – Geelong TerritoryJoin IQVIA and be part of launching an innovative new product. IQVIA has an exciting opening for an enthusiastic and ambitious Medical Sales Representative to join our high‑performing team. This role covers the Geelong Territory, offering the opportunity to build strong relationships across a diverse territory while promoting an innovative, market‑shaping product. About the RoleAs a key member of our sales team, you'll play a pivotal role in driving product growth and fostering advocacy among key healthcare professionals. Reporting to the State Sales Manager, your focus will be on engaging General Practitioners and ensuring strong support for our breakthrough therapy - ultimately contributing to improved patient outcomes. What You’ll Be DoingDevelop and deliver a strategic territory plan to maximise value and drive sustainable growth. Achieve and exceed sales targets and marketing objectives across the assigned product portfolio. Build and maintain strong, commercially driven relationships with GPs and key stakeholders. Support the rollout of key programs that strengthen our brand and market presence. Deepen your expertise by mastering product knowledge and understanding the associated disease area. Preferred QualificationsTertiary education in Science or Business is advantageous. Previous sales experience - particularly in GP Sales, Diabetes, or new product launches - is valued but not essential. Strong B2B sales capability and the ability to operate autonomously across a broad territory. Familiarity with the Geelong region and willingness to travel. What Makes You Successful in This RoleConfident, persuasive communicator with excellent presentation skills. Quick thinker with the ability to adapt in a fast‑paced, dynamic environment. A commitment to professionalism, ethics, and delivering exceptional service. Proven success working in a target‑driven environment. Strong networking, planning, and strategic relationship‑building abilities. If you’re motivated, driven, and excited by the opportunity to develope your career in pharmaceutical sales, we’d love to hear from you. Apply now with your CV, and a member of our Talent Acquisition team will be in touch with next steps. 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.

Essential Functions Under general supervision, perform site activation activities in assigned studies for investigative sites, according to applicable regulations, SOPs and work instructions, working closely with the  Site Activation Manager (SAM), Project Management team, and other departments as necessary. Review documents for completeness, consistency and accuracy, under guidance of senior staff.Prepare site regulatory documents, reviewing for completeness and accuracy.Inform team members of completion of regulatory and contractual documents for individual sites.Distribute completed documents to sites and internal project team members.Support the updating and maintenance of internal systems, databases, tracking tools, timelines and project plans with accurate and complete project specific information.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.Qualifications Bachelor's Degree Life sciences or a related field1 years’ experience in a healthcare environment or equivalent combination of education, training and experience. Productive individual contributor who works under general supervision. Problems faced are generally routine but may require interpreting procedures or policies to resolve.Good interpersonal communication and organizational skills.Good word processing skills and knowledge of MS Office applications.Good attention to detail.General awareness clinical trial environment and drug development process.Ability to work on multiple projects.Ability to establish and maintain effective working relationships with co-workers, managers and sponsors.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.

We are seeking Manager, Laboratory Biotech Services - Remote to join IQVIA Laboratories at Marietta, GA.We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose, join us as we transform and accelerate research and development. Job Summary:Lead the day-to-day direction of a Client Delivery Team to achieve client and company goals while supporting staff development and operational excellence. In this role, you will drive compliant study execution, strengthen client relationships, and step into project management responsibilities as needed to ensure high-quality delivery. What You'll Be Doing:Lead assigned staff and oversee daily team activities in line with organizational policies and applicable regulationsCoach, mentor, and develop team members while supporting performance management and professional growthDrive continuous improvement in project delivery processes to promote consistent, high-quality customer serviceEnsure studies are planned and executed in accordance with FDA, ICH, and/or EMEA guidelines and Good Clinical Practice requirementsBuild and maintain strong sponsor relationships while serving as a liaison between Project Services, internal teams, external vendors, and clientsParticipate in customer meetings, bid defense activities, and governance discussions to support new and repeat businessMonitor productivity, quality, and contract performance metrics and report outcomes to leadership What We Are Looking For:Bachelor's Degree in Life Sciences and/or related field preferredMinimum 4 years of experience in clinical trials/ hospital-funded research, project management or laboratory environmentDemonstrated computer proficiency with Microsoft Office and company systems, or equivalent experience with similar Centralized Laboratory systems preferredStrong knowledge of Project Services processes, company laboratory processes, and/or equivalent working knowledge of central laboratory operations preferredOther equivalent combination of education, training, and experience may be accepted in lieu of degree The Knowledge, Skills and Abilities Needed for This Role:Strong people management skills with the ability to develop and lead cross-functional teamsExcellent interpersonal, organizational, and client management skills with the ability to meet deadlines in a fast-paced environmentStrong written and verbal communication skills and the ability to establish and maintain effective working relationships with coworkers, managers, and clients What We Offer You:We put our employees at the center of everything we do and are committed to providing them, and their families, with benefits that meet their diverse and changing needs. We invest in integrated benefits programs and resources to take care of our employees' physical, mental and emotional, financial and social well-being so they can thrive at home and at work, at any stage of their well-being journey.To learn more about our benefits, visit https://jobs.iqvia.com/benefits.If you're looking to unleash your potential, join IQVIA Laboratories to help make the extraordinary possible!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 $83,000.00 - $173,000.00. 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.

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. Für ein spannendes Projekt im Bereich Diabetes suchen wir Pharmareferenten als Portfolio-Spezialist Metabolic Care (m/w/d) Im Gebiet: Herborn, Wetzlar, Marburg, Frankenberg, Nidda, Fulda, Schlüchtern Das sind Deine Aufgaben: Als Portfolio Spezialist (m/w/d) bist du dafür zuständig, fundierte Informationen zu deinem Produktportfolio im Bereich metabolischer Erkrankungen sowie den Dienstleistungen professionell zu vermitteln. Dabei übernimmst du innerhalb deines zugewiesenen Gebiets, der Produktsparte oder für ausgewählte Kunden im Bereich niedergelassener Allgemein- und Fachärzte eine Vielzahl spannender Aufgaben: Eigenständige Planung, Durchführung und Analyse von Kundenkontakten sowie Erstellung eines gebietsspezifischen Aktivitätenplans. Umsetzung der nationalen Sales- und Marketingstrategie und Aufbau nachhaltiger Beziehungen zu Zielkunden. Verantwortung für den wirtschaftlichen Erfolg der Fokusprodukte und die Organisation regionaler Fortbildungen (Präsenz & Digital). Aktive Mitwirkung an Tagungen, Meetings und Awareness-Kampagnen, um Innovationen und Pipeline-Produkte zu fördern. Sorgfältige Dokumentation aller Aktivitäten im CRM-System und kontinuierliche Weiterbildung durch interne und externe Trainings. Das bringst Du mit: Du bist geprüfter Pharmareferent (m/w/d), Pharmaberater (m/w/d) oder bringst eine vergleichbare Qualifikation gem. §75 AMG mit (z. B. durch ein naturwissenschaftliches Studium). Erfahrung im Pharma- oder Medizintechnikvertrieb wünschenswert. Interesse an neuen innovativen Produkten und deren Platzierung im Markt. Ausgeprägte Kommunikationsstärke im Umgang mit unterschiedlichen Zielgruppen sowie eine klare wirtschaftliche Ziel- und Kundenorientierung. Du möchtest etwas bewegen – für Dein Präparat, für dich selbst und vor allem für betroffene Patienten. Ausgeprägte soziale Kompetenz und Teamfähigkeit. Sehr gute kommunikative Fähigkeiten sowie die Bereitschaft, eigenverantwortlich und ergebnisorientiert zu arbeiten. Du verfügst über ein ausgeprägtes digitales Know-how gepaart mit IT-Kompetenz. Fließende Deutschkenntnisse in Wort und Schrift sind Voraussetzung. Das erwartet Dich bei uns: 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] #LI-CES #LI-DNP #LI-SS2 #Pharmaberater #Biologie #Chemie #Pharmareferent #BTA #CTA #PTA #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.

IQVIA is expanding its team and is now seeking an additional Medical Science Liaison based in Spain. This is one of several newly created roles across the EU due to our customer’s ongoing success, and ahead of product launches in 2026.  Our customer is a global biopharmaceutical company, dedicated to bringing biosimilar medicines to market, ensuring high-quality biologics are available to more patients at cost effective prices.  Since their inception they have developed the industry’s most rapidly advancing biosimilar medicines portfolio and become leaders in this field. This a fantastic opportunity to contribute to the medical strategy in a company which operates in diverse, highly specialist therapy areas and which continues to demonstrate significant growth. Territory to cover: Spain and Portugal You’ll be joining an established MSL in the region, and the two of you will team up to cover Spain and Portugal. In this role, you will: Engage with customers through scientific discussions, presentations, and education, with responsibility for half of Spain and the southern region of Portugal.Provide medical information and responses to complex medical questions from clinicians.Offer internal scientific support and training, serving as an expert resource for commercial colleagues.Coordinate scientific education activities and participate in events such as Advisory Boards and congresses.Support investigators and interact with scientific societies and patient groups.Collect and report relevant insights to the company, such as competitor information and treatment patterns.Contribute to the design and delivery of the Medical Plan for Spain and Portugal.Gather and report medical and congress intelligence.Develop local publications and maintain monthly contact with the Medical Director and HQ Medical team.Identify and develop KOLs, providing educational and scientific support as needed.Collaborate cross-functionally with the Commercial Department and Country Managers.Qualifications: Scientific degree (PhD, PharmD, MD, MSc, etc.).Must have previous pharmaceutical industry experience as an MSL in Spain.Strong leadership and collaboration skills, with the ability to influence stakeholders.Fluency in Spanish, and strong English language skills.Based in Spain with a full driving license.#LI-CES #LI-VK1 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.

Role Summary: Serve as the designated Local Contact Person for Pharmacovigilance (LCPP) in Spain, ensuring compliance with Spanish and EU pharmacovigilance regulations. Act as the primary liaison with local health authorities and support the Qualified Person for Pharmacovigilance (QPPV) in maintaining the pharmacovigilance system. Additionally, lead global process ownership for assigned PV processes, driving standardization and continuous improvement across regions.   Key Responsibilities: Local Pharmacovigilance Responsibilities (Spain): Act as the Local Contact Person for Pharmacovigilance in Spain, available 24/7 for urgent safety issues.Ensure compliance with Spanish PV requirements, including local reporting obligations and maintenance of local PV documentation.Serve as the primary interface with Spanish health authorities (e.g., BfArM) for pharmacovigilance-related queries and inspections.Maintain awareness of local regulatory changes and implement necessary updates to PV processes.Support the EU QPPV in oversight of the PV system and ensure alignment with the Pharmacovigilance System Master File (PSMF).Additional Responsibilities: Prepare and maintain PSMFs and local annexes for Spain.Oversee development and negotiation of pharmacovigilance agreements for assigned clients.Act as EU QPPV for small clients, where applicable.Mentor and train team members on PV processes and regulatory requirements.Support audits and inspections at global and local levels.Qualifications: Education: Bachelor’s degree in Life Sciences, Pharmacy, Medicine, or related field (advanced degree preferred).Experience:Minimum 5 years in pharmacovigilance or drug safety within a pharmaceutical company or CRO.At least 3 years of experience in PV system management and regulatory compliance.Previous experience as LCPP or similar role in Spain strongly preferred.Knowledge:In-depth understanding of EU and Spanish PV regulations (GVP Modules, AMG requirements).Strong knowledge of PV agreements, PSMF, and risk management processes.Skills:Excellent communication skills in English and Spanish (written and verbal).Strong organizational and time management skills; ability to manage multiple priorities.Effective stakeholder management and relationship-building skills.Ability to lead process improvement initiatives globally.Additional Requirements: Availability for 24/7 contact as required by Spanish PV regulations.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.

Te apasiona la venta y el contacto directo con farmacias? 🚀 ¿Eres un perfil claramente comercial y orientado a resultados? ¡Esta es tu oportunidad!Buscamos un/a Delegado/a de Ventas con experiencia en canal farmacia 💼 para gestionar la zona de Valencia, Alicante y Murcia, con base en Valencia, incorporándose a un proyecto dinámico y en crecimiento 📈.Tu día a día estará enfocado en la gestión y desarrollo de la cartera de farmacias 🤝, identificación de oportunidades de negocio, negociación y cierre de acuerdos, con un claro enfoque a resultados y posicionamiento de producto en el punto de venta.Buscamos una persona con alta capacidad comercial 🔥, proactiva, ambiciosa y acostumbrada a trabajar por objetivos, que destaque por su habilidad para generar relaciones de confianza con el cliente y dinamizar las ventas en su zona.Se ofrece la oportunidad de formar parte de un proyecto estable, con recorrido y potencial de crecimiento 🌱, donde podrás desarrollar al máximo tu perfil comercial.Si buscas un entorno donde potenciar tu perfil comercial, asumir retos y crecer profesionalmente, queremos conocerte 💼✨📩¡Da el siguiente paso en tu carrera y únete a un proyecto con impacto real en farmacia! 🚀Requisitos🎯 Perfil que buscamos-Formación universitaria en Ciencias de la Salud.-Experiencia mínima de 2 años como delegado/a de visita a farmacia.-Residencia en la zona de influencia.-Carnet de conducir y disponibilidad para desplazarte dentro del territorio asignado.💡 Competencias clave para brillar en este rol-Excelente comunicación y capacidad para generar relaciones de confianza.-Orientación al cliente y sensibilidad hacia sus necesidades.-Fuerte capacidad de análisis para entender el negocio y detectar oportunidades.-Planificación y organización para gestionar eficientemente tu zona.-Espíritu de trabajo en equipo, sumado a una actitud proactiva e iniciativa constante.-Clara orientación a resultados y motivación para alcanzar objetivos comerciales.Tipo de contrato:Temporal 6 meses con posibilidad de continuidadNúmero de vacantes:1Remuneración anual: 26.000 € brutos fijo año & 24.500 € Incentivos#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 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.

Senior Set-Up Coordinator IQIVIA Laboratories Home-based, office-based, hybrid options available   IQVIA Laboratories is a global leader in drug discovery and development laboratory services, offering a comprehensive suite of central laboratory and specialty biomarker services. Our expertise spans genomics, immunoassays, flow cytometry, anatomic pathology, precision medicine assays, vaccine assays, ADME, and bioanalytical services. IQVIA Laboratories also specializes in antibody and biomarker discovery, as well as decentralized clinical trial laboratory solutions. Committed to scientific rigor and operational excellence, we support every phase of the drug development and discovery process across diverse regions and regulatory frameworks, ensuring the highest standards of data integrity and accelerating the delivery of transformative therapies to patients.  Join us on our exciting journey!    Job Overview:  Manage the end‑to‑end design and implementation of protocol amendments and sponsor‑driven changes, ensuring alignment with system capabilities and regulatory requirements. Identify and apply AI‑enabled tools, automation, and data analytics to improve study set‑up efficiency, data quality, and amendment delivery. Lead the design, configuration, and validation of laboratory databases and study set‑up activities using advanced Clinical Trial Management Systems (CTMS) and related digital platforms. Communicate effectively with Sponsors and CROs, providing expert input on technology‑enabled study design and delivery. Maintain ownership of amendment delivery, sponsor deliverables, and database quality while proactively identifying opportunities to enhance ways of working through AI, digital transformation, and innovative thinking. Develop, plans, and delivers laboratory project setup and execution activities across the full study lifecycle, ensuring alignment with sponsor requirements, regulatory standards, and organisational quality expectations. Requirements:   Bachelor's Degree Life sciences or related field1+ years relevant experience (Clinical, Medical or Healthcare industry preferred) orequivalent combination of education, training and experience.Demonstrated interest or experience in AI, automation, data analytics, or digital transformation within clinical or laboratory environments.Strong working knowledge of Clinical Trial Management Systems (CTMS) and laboratory data systems, with the ability to adapt quickly to new technologies.Comfortable working in fast‑paced, evolving environments where new tools and approaches are continuously introduced.Curious, proactive, and motivated to explore emerging technologies and innovative solutions.Join IQVIA to see where your skills can take you   Global exposure  Variety of therapeutic areas Collaborative and supportive team environment  Access to cutting-edge and innovative, in-house technology Excellent career development and progression opportunitiesIQVIA 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. 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.

FSP Senior Epidemiologist (Oncology) Core Function Description: Design and conduct epidemiological studies to generate real-world evidence within time, budget, and quality standards, including but not limited to natural history of disease, population characterization, assessment of treatment patterns and unmet need, development of external comparators, benchmarking of clinical outcomes, comparative safety and effectiveness research, and post-authorization studies. Skill sets of the Epidemiologist role are similarly required, with the expectation of more experience, able to operate strategically under limited supervision, well versed in current Epidemiology research methods, deep understanding of how RWE fits within drug development, regulatory, medical, safety and other functions. Required Experience Lead development of study protocols, analysis plans, and study reports to answer research questions of priority to RWE.Lead, design, and manage epidemiological, biomarker and/or data science projects.Lead, plan, design, and conduct analyses for internal and external decision making (e.g., responses to regulatory authorities, rapid analyses of safety queries).Lead the identification of fit-for-purpose data for the timely execution of the RWE strategy.Constructed cohorts using RWD sources (e.g., claims, EHR) and evaluate key variables, including diagnosis and procedures codes, and plan validation studies as needed.Contribute to the communication of observational research results and methods, including development of pertinent sections of regulatory documents, reports, publications, white papers.Support the effective communication of study/analysis results to support internal and external decisions.Coauthor abstracts and manuscripts for external dissemination of methodologic study results.Contribute to the development of processes and training aimed at increasing the efficiency, quality, and impact of functional activities.Technical Expertise: Observational research methods (both Primary and Secondary), deep knowledge of biostatistics and analysis methods, understanding of regulatory processes.Ability to design studies independently, (i.e., ability to translate research questions to create study design).Subject Matter Expertise: Extensive experience conducting cancer epidemiology studies (solid tumor experience a plus), experience with commercial Oncology EMR databases.Leverage RWE expertise to identify evidence gaps and develop options to address the evidence gaps in support of Clinical Development Programs in early phase (ph1/2).Provide subject matter expertise and conduct analyses for descriptive and comparative research using RWD (examples include claims, EHR, registry data) for methodologic research questions.Expert knowledge and extensive experience with cancer epi (solid tumor experience a plus), extensive experience with oncology EMR databases, extensive experience with conducting cancer epi studies.Experience with Clinico-genomic multi-modal data (e.g., Tempus AI) or population biobank data (UK biobank) is a plusMinimum Qualifications PhD in Epidemiology, Biostatistics, Psychometrics, or related field with a minimum of four (4) years of relevant post-doctoral experience, preferably in pharmaceutical industry, biotechnology, or consulting environment. Master’s degree in epidemiology, biostatistics, bioinformatics, or relevant scientific field, plus 7-9 years of experience in lieu of PhD may be acceptable.Deep understanding of observational research methods and experience to support the design and conduct of observational research, including protocol, statistical analysis plan, and study report development.Extensive knowledge of secondary data sources and experience with secondary data analysis, including electronic medical record and/or medical claims databases.A record of scientific publications demonstrating expertise in observational study design, analysis, and interpretation is preferred.Demonstrated ability to function with an increasing level of autonomy and to develop productive cross- functional collaborations in a matrix environment.Ability to manage priorities and performance targets.Experience in leading drug development project for 2+ years for therapeutic area of assignment 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 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 $125,800.00 - $350,300.00. 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.

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 OverviewProvide advanced technical expertise to develop and maintain programs to meet internal and external clients’ needs.  Plan and lead the development of project-related solutions to the full scope of statistical programming tasks.  Provide technical expertise to the Statistical Programming department. Essential Functions• Perform and plan: (i) the programming, testing, and documentation of programs for use in creating statistical tables, figures and listing summaries, (ii) the programming of analysis databases (derived datasets) and transfers of data for internal and external clients. May perform and plan the programming of database quality control checks.• Program the integration of databases from multiple studies or sources.• Develop programming documentation including plans and specifications, as appropriate.• Provide advanced technical expertise in conjunction with internal and external clients, and independently bring project solutions to teams and department.• Perform and plan the development, implementation and validation of new process technologies, macros and applications.• Fulfill project responsibilities at the level of statistical team lead for single studies, under supervision.• Understand the Scope of Work, estimate the work completed, and manage Out of Scope for single studies. May manage budget and resource requirements and provide revenue and resource forecasts for single studies. May be required to understand budget and quote assumptions.• Provide training and guidance to lower level and new staff. Qualifications• Master's Degree Computer science or related field and 1 year relevant experience Req Or• Bachelor's Degree Computer science or related field and 2 years relevant experience Req• Equivalent combination of education, training and experience Req• Knowledge of statistics, programming and/or clinical drug development process• Working knowledge of computing applications such as Base SAS, SAS/STAT and SAS Macro Language• Good organizational, interpersonal, leadership and communication skills• Ability to effectively handle multiple tasks and projects• Excellent accuracy and attention to detail• Ability to establish and maintain effective working relationships with coworkers, managers and clients 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.