IQVIA

Job Level: Medical Director, Neurologist Time Type: Part Time (20 Hrs/week) Location: Home-based in the U.S. or Canada Job OverviewThe Medical Director will be the medical expert on the IQVIA team working on clinical research trials in neurological diseases and disorders. This involves applying medical and scientific knowledge and expertise in support of the trial. These clinical trials will cover the full range of neurologic disorders.  Essential FunctionsThe role includes predominantly Medical Monitoring responsibilities with Medical Strategic input involvement as requested. Medical Monitoring: Primarily serves as Medical Monitor (at the global or regional level) on assigned clinical trials.Serves as Scientific Advisor (providing medical advice and input) to Project Leaders on the medical and scientific aspects of assigned projects.Provides medical support to investigative sites and project staff for protocol-related issues including determining if subjects are eligible to participate in given clinical trials.Provides therapeutic area/indication training for the project clinical team.Attends and presents at Investigator Meetings.Performs review and clarification of trial-related Adverse Events (AEs).Attends Kick-Off meetings, weekly team meetings, and client meetings, as needed or requested.Responds to urgent protocol-related issues at investigative sites.Medical Strategy: Contributes to the development of the medically-related aspects of client proposals including the budget related to medical monitoring.Provides medical and scientific advice and guidance to key internal stakeholders developing proposals: this may include reviewing the protocol for scientific/regulatory soundness and feasibility, identification of target site and principal investigator profiles, anticipated patient recruitment, standard of care and competitive landscape.Attends and presents at bid defense meetings, as required.Requires 5-10 % periodic regional and international travel.Qualifications Medical degree from an accredited and internationally recognized medical schoolBoard certified or eligible in NeurologyIdeally candidate will have a minimum 2 years clinical trials experience as an investigator or medical /clinical expert in the Pharma, CRO, or Biotech industry.Ability to establish and maintain effective working relationships with coworkers, managers and clients.Strong communication, presentation and interpersonal skills, including good command of English language (both written and spoken).Robust and current knowledge of scientific, clinical, regulatory, commercial and competitive landscape in Neurology.Proven skills in providing consultation and advice on multiple assignments are required, as well as initiative and flexibility.Availability for intermittent domestic and foreign travel to support these business assignments.Subspecialty interest and training in neuromuscular diseases (ALS, myasthenia gravis, neuropathy), or sleep disorders, or pediatric neurology is a plus, but not required.Has the skill, knowledge, and training necessary to provide medical monitoring for the full range of neurological diseases/disorders. #LI-Remote #LI-NITINMAHAJAN 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 $154,900.00 - $431,500.00. 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.

Patient Access Specialist Position Summary The Patient Access Specialist serves as the primary point of contact for patients, healthcare providers, and field representatives within a Patient Support Services (PSS) program. This role is responsible for facilitating patient access to therapy by conducting benefit investigations, verifying insurance eligibility, supporting prior authorizations and appeals, and assisting with copay and patient assistance programs. Patient Access Specialist support patients throughout their treatment journey while ensuring a high level of service, compliance, and coordination across stakeholders. This role will be a contract role with IQVIA managed by an external agency, with the opportunity to be converted to an IQVIA full-time employee. Job Responsibilities Serve as the primary point of contact for patients, providers, and stakeholdersConduct inbound and outbound calls to support program servicesPerform insurance benefit investigations and verify coverageSupport prior authorizations and appeals processesAssist with copay and patient assistance program enrollmentProvide ongoing patient support and adherence coordinationDocument all interactions accurately and timelyDeliver high-quality customer service across communication channelsCollaborate with field representatives and internal teamsManage patient caseloads with timely follow-upEnsure compliance with HIPAA and regulatory requirementsIdentify and report adverse events and product complaintsTroubleshoot issues and escalate as neededMaintain knowledge of program policies and processesSupport onboarding and training of new employeesMeet quality standards and KPIsPerform additional duties as assignedSchedule Available for an 8-hour shift between 8:00 AM – 8:00 PM EST8:00 AM – 5:00 PM EST9:00 AM - 6:00 PM EST11:00 AM - 8:00 PM ESTAbility to work varying shifts, including evenings as neededRemote role requiring a compliant home workspaceRequired Qualifications High School Diploma or equivalent3–5+ years of experience in medical billing, reimbursement, or insurance verificationRobust understanding of payer coverage and reimbursement (medical and pharmacy)Experience in a contact center or patient support environmentProficiency with Microsoft Office and CRM systemsStrong written and verbal communication skillsHigh attention to detail and multitasking abilityAbility to work independently in a virtual environmentProblem-solving and solution-oriented mindsetKnowledge of HIPAA and data privacy requirementsMust reside in the country where the role is postedPreferred Qualifications Associate or Bachelor’s degreeExperience in a Patient Support Services (Hub) environment with focus on rare diseasesHealthcare or pharmaceutical customer service experienceThis role is posted under a market-aligned title to better reflect the scope and candidate profile. The internal title for this position is Care Manager within PASS. #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 29.81 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.

Join IQVIA and lead high-impact clinical projects that drive innovation and improve patient outcomes worldwide. We are seeking a strategic and people-focused leader to oversee global CPM teams, ensuring delivery excellence, strong financial performance, and exceptional client satisfaction. Role OverviewIn this senior leadership role, you will provide oversight of CPM teams and corporate initiatives, driving productivity, quality, and on-time delivery across complex clinical programs. You will partner closely with clients and internal stakeholders to bring strategic direction, leverage therapeutic expertise, and ensure operational excellence across global teams. You will also play a critical role in developing talent, building high-performing teams, and fostering a culture of accountability, collaboration, and continuous improvement. Key ResponsibilitiesLead and develop a team of CPM managers, ensuring delivery of clinical programs on time, within budget, and to quality standardsDrive operational excellence through strong project oversight, risk management, and performance monitoringCoach and mentor leaders on project execution, problem-solving, and strategic planningEnsure alignment with global processes, tools, and best practicesMonitor project metrics and proactively address risks, quality issues, and resource needsPartner with clients to provide guidance on clinical development strategy and deliveryContribute to corporate initiatives and act as a cross-functional leader within IQVIAAttract, develop, and retain top talent while supporting ongoing learning and developmentQualificationsBachelor’s degree in life sciences or related field~15+ years of clinical research experience, including significant leadership in global/multi-regional environmentsDeep knowledge of clinical trials, GCP/ICH guidelines, and the clinical research landscapeProven ability to lead teams, influence stakeholders, and deliver complex programs successfullyStrong business acumen, including project financials and performance metricsExcellent communication, collaboration, and leadership skillsWhat We’re Looking ForA strategic leader who can balance operational delivery with long-term visionStrong people manager with a passion for coaching and developing talentAbility to navigate complexity, drive results, and build strong client relationships in a global environmentIQVIA 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 $125,900.00 - $394,400.00. 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.

Job OverviewUnder direct supervision, assists in providing systems support in developing and enhancing business systems to provide new or enhanced products to clients or effective planning, reporting, and analysis tools to internal functions. Essential Functions Assist in defining system scope, objectives, and business needs through research, fact-finding, and analysis of business/system requirements.Analyze business and user needs, document requirements (user stories/functional requirements/acceptance criteria), support clarifications, and help track requirement changes/priorities as needed.Perform hands-on configuration within the company’s solution platform based on approved requirements and client-provided documentation/inputs, under guidance where needed.Participate in client and internal discussions for clarifications, walkthroughs, and solution alignment; communicate clearly and professionally with stakeholders.Create and maintain Jira tickets (scope, owner, due dates, dependencies) and keep status updated regularly to drive work items to completion.Support testing and UAT activities: prepare test scenarios, support execution, log defects, assist triage, and capture evidence as required.Perform basic root cause analysis (RCA) for reported issues/defects (with guidance), document findings clearly, and coordinate fixes/changes through the tracking process.Support go-live and release activities for new enhancements, including readiness checks, validation, coordination with stakeholders, and post-release verification.Support end-to-end release execution activities (under guidance), ensuring required steps, documentation, and tracking are completed as part of the release process.Maintain Confluence documentation / knowledge-transfer (KT) artifacts (project notes, configuration notes, release notes, KT pages) to reduce dependency on individuals and improve cross-team continuity.Support basic reporting needs, including learning and creating/validating reports within the Admin Console and assisting with ad hoc status/reporting requests.Support transition of enhancements/features from delivery into support or specific processes where applicable.Proactively identify and flag risks, dependencies, and scope gaps early, and seek clarifications to reduce rework and late escalations.Contribute to team enablement by sharing learnings/KT with the team when ready (post ramp-up)Qualifications Bachelor's Degree Life Sciences / Economics / Business Pref OrMaster's Degree Life Sciences / Economics / Business Pref OrPh.D. With commercial experience in the healthcare industry PrefWorks willingly and effectively with others in and across the organization to accomplish team goals. Knowledge and understanding of the fundamental processes of business, their interaction, and the impact of external/internal influences on decision making, growth and decline.Knowledge of consulting methods, tools and techniques, related to one’s functional area. Healthcare IT / Digital HealthBusiness AnalysisRequirements GatheringFunctional Requirements Gathering and DocumentationPublic Health / Registry ExposureData ValidationReporting / DashboardingIQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

The Team IQVIA is a fast-growing and highly successful consultancy business, focusing on delivering tangible business results to our clients who are key decision-makers and business managers across the international pharmaceutical and healthcare industry. With direct access to the world's most comprehensive healthcare information, analytic and research resources, IQVIA experts design and deliver innovative, data- and technology-enabled evidence programmes for the pharmaceutical industry. We apply scientific rigour and advanced analytics to real-world data to help our clients improve healthcare. The IQVIA Global Health Economics and HTA team includes highly qualified multi-disciplinary professionals in a variety of health economics, statistics, life sciences and epidemiology-related disciplines based across multiple geographies worldwide. We help our customers design and execute an evidence generation strategy meeting payer and health technology assessment (HTA) evidence requirements and effectively communicate their product's value story. Our clients operate in the life sciences industry, including the global top 20 pharmaceutical companies, medical device and biotech companies, as well as public health providers and regulatory authorities. They are looking for insight and evidence around the safety, efficacy, effectiveness and cost-effectiveness of healthcare delivery systems, medical devices, and pharmaceutical products spanning the full spectrum of therapeutic and disease areas. Our diverse mix of clients, the breadth of disease areas, as well as increasing access to novel data sources and methodologies provide a constant and rewarding challenge for our people. For more information about our company please visit our website: https://www.iqvia.com/ Role Overview This is a manager role within the IQVIA Global Health Economics and HTA team with a focus on health technology assessment (HTA) and strategic offerings to support our clients with designing an evidence generation and dissemination strategy for their products that meets HTA requirements and optimises the chances for market access. The primary focus of this role is on UK HTA, supporting submissions and engagements with agencies such as NICE and the SMC, although there is flexibility to work on other types of products and geographies should the opportunity arise. The successful candidate will: Be involved in shaping and leading the team and offerings, working closely with the wider senior leadership team and centres of excellence across the global network Manage business development, from proactively developing client relationships to understanding their strategic goals and milestones, with senior oversight; confirming, managing and maintaining the scope of the project to meet those goals in a timely and efficient manner Manage HTA project strategy and direction, with a particular emphasis on UK HTA processes and requirements, with senior oversight; identifying potential challenges to product value, and the development of risk mitigation strategies, as appropriate Manage the project delivery team on a range of projects, including dossier development and submission support for UK HTA agencies, early scientific advice, informing and defining HTA strategy and other strategic HTA offerings to support our clients, with senior oversight. There will also be opportunities to contribute to multi-country and global HTA projects Involvement in mediating, negotiating and problem solving, within and outside of the immediate project team, with senior oversight Train and identify opportunities for more junior members of the team to support their career development as HTA specialists Work within and across internal IQVIA teams, including technical consultants responsible for studies generating HTA evidence and complementary functions such as Market Access, Patient-Centered Solutions, HTA Accelerator Solutions, database studies and local teams across the global network Liaise with clients who will include pharmaceutical, biotechnology and medical devices companies with global and regional headquarters, and occasionally their affiliate teams Support and/or lead thought leadership for HTA topics, such as preparing conference abstracts and posters, supporting development of white papers and peer-reviewed publications on HTA and guiding interns working with the team on HTA-focused thesis topics Provide line management, depending on interests The demand for IQVIA's HTA offerings has seen dramatic increases over the past two years and will continue to expand in response to evolving HTA processes globally, including the growing importance of UK HTA. The role of the Senior Consultant is a management role within the IQVIA Global Health Economics and HTA team and is expected to play an important role in shaping the team's UK HTA offerings. There will also be opportunities to expand your portfolio into other areas if desired. The role is based in either Spain, Greece, Portugal or South Arica, with flexibility regarding frequency of office and home working. Please refer to our diversity and inclusion statement for further information. The Successful Candidate We are looking for a candidate with a good mix of academic and professional experience, domain experience, and interpersonal skills. An ideal candidate has experience with UK HTA submissions and preparing for and supporting early HTA scientific advice, as well as proven success in navigating HTA processes in a strategic way to optimise a product's access to markets and reimbursement. Experience with multi-country HTA submissions is also highly desirable. Experience with statistical methods used in clinical trials and evidence synthesis is highly desirable. The ideal candidate will also have a good understanding of the structure typical of our clients from the pharmaceutical industry and how to successfully navigate this structure to achieve client's aims. The list below should be viewed as a guide rather than a checklist. Qualifications and Desired Experience Postgraduate degree level education or higher from a relevant discipline (such as, but not limited to, HTA, health economics, economics, life sciences, epidemiology, biostatistics, public health, medicine, pharmacy, etc.) AND at least 4 years of relevant work experience (such as, but not limited to, pharmaceutical sector, consulting, academia) with preparing evidence submissions aligned to the HTA processes and requirements within the UK and/or Europe as well as involvement in the appraisal and negotiation processes, where relevant Demonstrable commercial awareness and thorough understanding of the pharmaceutical industry, with an existing network of HEOR contacts highly desirable Project management experience, including managing multidisciplinary teams Strategic thinking and attention to detail Previous experience in a consultancy environment is highly desirable Commercial acumen and proven consultancy skills is highly desirable Strong written and verbal communication skills with fluency in English – applications should be sent in English Strong understanding of the design of clinical trials, statistical methods used in clinical trials, and methodology for evidence synthesis is highly desirable Quantitative skills, including biostatistics and health economic modelling methods and good knowledge of statistical software packages (e.g., STATA, R) is desirable but not essential Please submit your CV in English. Our Commitment to You IQVIA are committed to your professional growth in the healthcare industry. During the first three months new joiners will be supported with a structured onboarding programme to ensure a smooth transition into the team and the wider organisation. IQVIA offers numerous training opportunities. As a Senior Consultant you will have opportunities for external trainings aligned with business and team objectives. IQVIA also offers unlimited access to eLearning courses on LinkedIn Learning and Learning Edge (our internal training platform). The organisational structure of the team ensures that each team member can have regular 1:1 meetings with their line manager. These meetings range from goal setting to advice for projects; the common theme is to provide personalised development support. You will be rewarded with a competitive salary, bonus, and benefits. You will have the opportunity to gain invaluable and transferable experience within an innovative team with a global footprint. Your new role offers flexibility, including remote working and occasional office visits. 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 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.

Overview IQVIA’s Financial Institutions Consulting (FIC) team advises investors (e.g. private equity, venture capital, hedge funds, etc.) on biopharma and life sciences investments, including commercial due diligence, asset and target screening, portfolio company growth strategy and exit/divestment strategy. Successful candidates will have the opportunity to engage with clients on high-profile investment decisions across a variety of industry-shaping transaction situations, business models and strategic issues. We operate in a multi-cultural, collaborative and fast-paced work environment, that is rich in development and growth. Role & Responsibilities As a Manager within IQVIA’s FIC team, you will be responsible for managing projects primarily in the areas of due diligence (buy- and sell-side), asset/portfolio/company valuation, asset screening and growth strategy Leverage consulting and transaction advisory experience, IQVIA information and expertise, and methodological know-how to manage projects that address client / business questions.Diagnose and understand complex strategic issues / diligence questions and structure project approach and team setup to address engagement objectivesManage project teams on a day-to-day basis through guiding research approaches, the design, development and delivery of client reports and presentations and QC of deliverablesServe as day-to-day point of contact with clients during project delivery – including presenting / communicating key project insights and recommendations – ensuring engagement satisfaction and supporting long-term enhancement of client relationshipsContribute to overall FIC team capabilities, including (but not limited to) the development of intellectual property, marketing materials, training, recruitment and go-to-market approachSupport Principals with business development, including proposal development and presentations.Serve as development lead of 3-4 team members, alongside supporting broader team developmentAbout You Candidates interested in joining IQVIA FIC as a Manager should have: Minimum of 5-6 years professional experience in strategy consulting, M&A/BD&L roles or within a financial institution (e.g. private equity, venture capital).Experience advising clients on commercial issues in the biopharma / life sciences industry and/or financial investors, including exposure to projects related to transactions / investments (due diligence, valuation, asset identification, growth strategy, forecasting)Project management experience in relevant domains, including managing large, multi-disciplined teams while maintaining high quality delivery. Demonstrated skills including project planning, workstream oversight, presentation/report development, quality control and client engagementStrong quantitative / analytical and qualitative research experience, supported by a problem solving mentality, keen eye for detail and critical thinking. Comfortable interpreting commercial / financial trends and results, with ability to guide teams to design and execute research and analysis and translate outputs into strategic implications for investorsWell-developed written and verbal communication skills including presentations, chairing meetings / Q&A sessions and report writingKnowledge of key issues and current developments in the biopharma / life sciences industryEvidence of career progression in consulting and/or transaction advisory rolesIn addition to the skills and experience above, a Manager should have: Bachelor’s degree or equivalent. MBA not required but a plusA track record of leadership and people developmentFluency in English (spoken and written)A willingness and ability to travel (where required)Right to live and work in the recruiting countryIQVIA 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.

Overview This role will form an important part of our Desktop Publishing team and will involve typesetting in various formats / languages as well as proofreading translated and localised layouts. The objective is to produce faultless, high-quality localised documentation. Job Scope To produce and deliver high quality layouts in multiple languages including: Typesetting / reformatting of foreign language manuals, product marketing materials and other project collateral Revision and proofreading of multilingual layouts to ensure quality and accuracy prior to client delivery Preparing files for localisation Analysing source files, preparing translation kits, integration, and QA Working closely with the project managers and clients to ensure project schedules are met Designing, documenting and implementing DTP processes Skills and experience Ideally a minimum of 2 years typesetting experience specially in MS Word and Adobe InDesign Comfortable working as part of a team and collaborating with other team members and departments across all job processes. Computer literate with a good knowledge of Windows and Adobe CC applications Skills in tools such as QuarkXpress, FrameMaker, Photoshop, Illustrator and Video editing would be an advantage but not essential as training will be provided Excellent attention to detail Good organisational and communication skills Knowledge of a foreign language, especially Asian or right-to-left languages, would be beneficial Enthusiasm and willingness to learn Flexible and adaptable to be able to work in a rapidly changing environment *Resume/CV must be submitted in English* #home-based #remote IQVIA is committed to embracing a diverse and inclusive work environment. Our goal is to attract and retain the best people, regardless of their gender, race, marital status, ethnic origin, national origin, age, disability, sexual orientation, gender identity or any other characteristic. Join us! 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.

Overview This role will form an important part of our Desktop Publishing team and will involve typesetting in various formats / languages as well as proofreading translated and localised layouts. The objective is to produce faultless, high-quality localised documentation. Job Scope To produce and deliver high quality layouts in multiple languages including: Typesetting / reformatting of foreign language manuals, product marketing materials and other project collateral Revision and proofreading of multilingual layouts to ensure quality and accuracy prior to client delivery Preparing files for localisation Analysing source files, preparing translation kits, integration, and QA Working closely with the project managers and clients to ensure project schedules are met Designing, documenting and implementing DTP processes Skills and experience Ideally a minimum of 2 years typesetting experience specially in MS Word and Adobe InDesign Comfortable working as part of a team and collaborating with other team members and departments across all job processes. Computer literate with a good knowledge of Windows and Adobe CC applications Skills in tools such as QuarkXpress, FrameMaker, Photoshop, Illustrator and Video editing would be an advantage but not essential as training will be provided Excellent attention to detail Good organisational and communication skills Knowledge of a foreign language, especially Asian or right-to-left languages, would be beneficial Enthusiasm and willingness to learn Flexible and adaptable to be able to work in a rapidly changing environment *Resume/CV must be submitted in English* #home-based #remote IQVIA is committed to embracing a diverse and inclusive work environment. Our goal is to attract and retain the best people, regardless of their gender, race, marital status, ethnic origin, national origin, age, disability, sexual orientation, gender identity or any other characteristic. Join us! IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

The Regulatory and Start-Up Specialist will perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include maintenance activities. Developing professional individual contributor who works under moderate oversight and supervision. Responsible for making recommendations for enhancements in systems and processes to solve problems or improve effectiveness of job area. Problems faced are general and may require understanding of broader set of issues but are not complex. Essential Functions• Under general supervision, serve as Single Point of Contact (SPOC) in assigned studies for investigative sites, Site Activation Manager (SAM), Project Management team, and other departments as necessary. Ensure adherence to standard operating procedures (SOPs), Work Instructions (WIs), quality of designated deliverables and project timelines.• Perform feasibility, site ID, start up and site activation activities according to applicable regulations, SOPs and work instructions. Distribute completed documents to sites and internal project team members.• Prepare site documents, reviewing for completeness and accuracy.• Ensure accurate completion and maintenance of internal systems, databases and tracking tools with project specific information.• Review and provide feedback to management on site performance metrics.• Review, establish and agree on project planning and project timelines. Ensure monitoring measures are in place and implement contingency plan as needed.• Inform team members of completion of fesibility, site ID, regulatory and contractual documents for individual sites.• Review, track and follow up the progress, the approval and execution of documents, questionnaires, CDA/SIF,  regulatory, ethics, Informed Consent Form (ICF), and Investigator Pack (IP) release documents, in line with project timelines.• Provide local expertise to SAMs and project team during initial and on-going project timeline planning.• Perform quality control of documents provided by sites.• May have direct contact with sponsors on specific initiatives. Qualifications• Bachelor's Degree Life science or related field• +1 years’ of relevant experience working in the regulatory department in Argentina: Local and regional committees - Initial submission, Amendments, Response to Pending Issues. ANMAT and CCIS - Initial submission (EFCA1) & ideally experience with list and calculation of medicines to be imported, Inclusion of centers (EFCA2), Amendments (EFCA3), Response to Pending Issues, IB Notification (EFCA4) ICF - Country and Site Specific Customization Essential Documents Collection TMF Update Trackers and Check lists. • Advanced level of English • Ability to work in a team #LI-NRJ 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 OverviewProject Leads are an integral part of clinical trial delivery, liaising with clinical teams to improve patients’ lives by bringing new drugs to the market faster. The Project Lead is an essential member of the core project team responsible for project delivery of clinical studies to meet contractual requirements in accordance with SOPs, policies and practices. Clinical Project Management is focused on project delivery, productivity and quality resulting in strong financial performance and customer satisfaction. Clinical Project leads can run their own studies. The Project Lead focus is on leveraging therapeutic expertise and IQVIA’s suite of solutions to drive operational excellence and strategic leadership with our customers. Essential Functions• Participate in bid defense presentations in partnership with Business Development and may lead the presentation for smaller, less complex regional studies.• May be responsible for delivery and management of smaller, less complex, regional studies.• Develop integrated study management plans with the core project team.• Accountable for the execution of clinical studies, or assigned portion of clinical studies, per contract while optimizing speed, quality and cost of delivery and ensuring consistent use of study tools and training materials and compliance with standard processes, policies and procedures.• Set objectives of the core project team and/or sub-team(s) according to agreed upon contract, strategy and approach, effectively communicate and assess performance.• Collaborate with other functional groups within the company where necessary to support milestone achievement and to manage study issues and obstacles.• Monitor progress against contract and prepare/present project and/or sub-team information proactively to stakeholders internally and externally.• Manage risk (positive and negative) and contingencies proactively and lead problem solving and resolution efforts.• Achieve project quality by identifying quality risks and issues, responding to issues raised by project team and/or sub-team members and planning/implementing appropriate corrective and preventative action plans.• May serve as primary or backup project contact with customer and would then own the relationship with the project’s key customer contacts, as well as communicate/collaborate with IQVIA business development representatives, as necessary.;• Build the cross-functional project team and lead their efforts; responsible for managing cross-collaboration of the core team and for overall project delivery to support milestone achievement and to manage study issues and obstacles.;• Ensure the financial success of the project.• Forecast and identify opportunities to accelerate activities to bring revenue forward.• Identify changes in scope and manage change control process as necessary.• Identify lessons learned and implement best practices.• May be assigned as the primary contact for vendors leading project vendor management and vendor management related activities as per project requirements.;• Adopt corporate initiatives and changes and serve as a change advocate when necessary.• Provide input to line managers of their project team members’ performance relative to project tasks.• Support staff development and mentor less experienced project team members on assigned projects to support their professional development.; Qualifications• Bachelor's Degree Life sciences or related field.• Around 6 years of experience in clinical research/project management. Minimum of 3 years in a Project Manager role in a CRO or pharma company. • Experience managing projects in these therapeutic areas: respiratory, ophthalmology, dermatology, rare diseases.• Communication - Strong written and verbal communication skills including good command of English language. Strong presentation skills.• Leadership - Ability to make decisions, bringing clarity to disparate information to inform actions and drive results.• Finances - Good understanding of project financials including experience managing, contractual obligations and implications. #LI-NRJ#LI-Remote 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.

Role Overview: The Site Enablement Solutions team at IQVIA provides qualified, clinically experienced research staff to clinical trial sites globally to accelerate and optimize the performance of clinical trials. By supplying sites with support for data entry, patient recruitment, patient visits, assessments, and other tasks, IQVIA is able to relieve the burden on trial sites and support our sponsors in completing their trials on time, and within budget. The goal of the Site Enablement Solutions Project Lead (SES PL) role is to optimize overall delivery of Site Enablement Solutions throughout the lifecycle of projects. The SES PL will also serve as internal consultants to the IQVIA study team and/or sponsor, present progress, and updates to sponsor, and manage overall delivery of our services on a project, including managing the Site Enablement project budget. Key Responsibilities Collaborate with pre- and post-award stakeholders to manage the coordination, planning, and implementation of Site Enablement Solutions.Develop global Site Enablement Solutions delivery strategy in identifying sites, executing on agreed upon scope and extending/expanding our services as warranted. Determine internal team resourcing based on study needs.Develop and execute operational plans on larger, multi- region studies or programs, including develop and implement risk management plans for minimizing impact on project objectives and deliverables. Establish study specific expectations and timelines.Communicate with sponsors and project teams to implement and monitor impact of Site Enablement Solutions.Provide ongoing proactive operational and tactical recommendations as needed based on study performance.Collaborate with internal and external teams to deliver site adoption and quality resource placement within specified timelines.Establish a collaborative approach for project delivery with Patient and Site Centric Solutions teams, including patient recruitment team and Direct to Patient Campaign. Schedule and facilitate internal study meetings.Represent Site Enablement Solutions at site/sponsor-facing meetings (i.e. KOM, IM, F2F/LL, etc.) to present strategy/rationale, and training.Ownership for study KPI and financial performance. Manage the scope of work, objectives, quality of deliverables, and other activities of assigned projects.Manage and oversee internal workflow management systems to ensure compliance.Other duties as assigned by management.Qualifications: Bachelors degree in life sciences or related field.Experience requires 3 - 5 years of prior relevant experience:5 years’ clinical trial experience3 years’ experience at a CRO or clinical trial services provider3 years in a Project Manager roleAdvanced level of English, you'll work with global projects and global teams.#LI-NRJ #LI-Remote 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 OverviewManage a team of clinical staff working in support of clinical studies to ensure projects are appropriately resourced and employees are trained and meeting project objectives.  Essential Functions Manage staff in accordance with organization’s policies and applicable regulations. Responsibilities include planning, assigning, and directing work, assessing performance and guiding professional development, rewarding and disciplining employees, and addressing employee relations issues and resolving problems.Participate in the selection for hiring new employees by conducting candidate review and participating in the interviewing process.Ensure that new employees are properly onboarded and trained.Ensure that staff has the proper materials, systems access and training to complete job responsibilities.Provide oversight for the execution of the training plan, SOP review and training experiences, as applicable.Participate in the allocation of resources to clinical research projects by assigning staff to clinical studies based on their experience and training.Manage the quality of assigned staff's clinical work through regular review and evaluation of work product.Identifies quality risks and issues and create appropriate corrective action plans to prevent or correct deficiencies in performance of staff.Ensures that staff are meeting defined workload and quality metrics through regular review and reporting of findings as outlined by clinical operations management.May collaborate with other clinical teams and other functional leadership to manage project related challenges and to achieve exemplary customer service.Participates in corporate or organizational departmental quality or process improvement initiatives.QualificationsBachelor's Degree in scientific discipline or health care preferred.Prior clinical trial experience including experience in a management/leadership capacity or equivalent combination of education, training and experience. In-depth knowledge of applicable clinical research regulatory requirements (i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines).Good leadership skills.Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint.Written and verbal communication skills including good command of English.Excellent organizational and problem-solving skills.Effective time management skills and ability to manage competing priorities. 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. The potential base pay range for this role, when annualized, is €41 600,00 - €62 400,00. 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.

As the only global provider of commercial solutions, IQVIA understands what it takes to deliver nationally and internationally. Our teams help biopharma get their medicines to the people who need them. We help customers gain insight and access to their markets and ultimately demonstrate their product's value to payers, physicians and patients. A significant part of our business is acting as the biopharma's field force to physicians or providing nurses to educate patients or prescribers. With the right experience, you can help deliver medical breakthroughs in the real world. We are excited to announce that we are looking for a Clinical Specialist to join our team of over 10,000 global field representatives in several regions making over 20 million product details annually for our pharmaceutical and biotech clients.   Operating Room Clinical Nurse The Biosurgery Clinical Specialist provides clinical assessments on adjunctive hemostat device needs, risks, recommendations and implementation recommendations to customers (primarily nurses, educators, risk managers, surgeons and techs).  This role plays an integral part in gathering key insights on utilization, techniques, applications based by specialty or service lines, capturing documenting and sharing these insights with the US Marketing team and partnering with local sales team to work collaboratively with sales management and the sales representative to gain appropriate access into aligned pilot accounts. Pivotal to the success of the candidate will be his/her ability to develop effective working relationships with the customers in the assigned territory. The incumbent must be able to work autonomously, be knowledgeable in adjunctive hemostats and confidently interact with clinical personnel and management.  The candidate chosen for this role will be expected to: Complete training on adjunctive hemostat devices and products to be proficient in product utilization and demonstration.Demonstrate mastery of all clinical information related to product application and the IFU; must be able to use this mastery to help drive and convert business by upgrading to more advanced brands. Develop strong, working relationships with surgical leadership and clinicians while providing adjunctive hemostat recommendations and bleeding risk assessments.  Educate OR nurses, techs and physicians on the proper techniques to effectively capture real-world utilization data by specialty/service lines.Conduct pilot account assessments, develop Analysis and present recommendations to management.Educate and inform end-users of clinical effectiveness of adjunctive hemostat products and technical aspects of Ethicon’s products.Present adjunctive hemostat recommendations and assist with implementation.Participate in adjunctive hemostat product evaluations as necessary within the aligned Pilot accounts.Assist field sales in collection of product utilization and performance data to support team business case.Present adjunctive hemostat continuing education programs to clinical and leadership groups within aligned accounts.Communicate educational content and distribute materials and programs. Assist US Marketing in identifying Key Opinion Leaders, upgrade opportunities and provide presentations of clinical data outcomes to end-users. Participate in key society meetings as appropriate.Requirements Qualifications/Experience 4 year Bachelor's degree required (degree in nursing, business or related field is preferred.)Valid RN license in state of residency requiredA minimum of 5 years clinical experience requiredA minimum of 3 years OR experience requiredStrong group presentation skills and experience in presenting clinical education and/or surgical leadership/management.   Specialty CNOR certification or related specialty is preferred.Excellent written and verbal communication skillsAssertive, ability to work independently and uncover opportunitiesAbility to plan and deliver formal presentations (large and small groups)Excellent written and verbal communication and organizational planning skills, including time and territory management and structured thinking in clinical procedure settings.Familiarity with AORN Surgical Smoke Safety GuidelinesStrong MS Office, Word, Excel skillsCompetencies The Biosurgery Clinical Specialist promotes the Ethicon culture through positive, ongoing customer relationships.This position also requires the ability to develop strong relationships with customers and within the Ethicon teamMust have the ability to work both as a partner with sales, marketing and commercial teammates and autonomously in the field, as needed.The ability to display decisiveness and an understanding of business acumen in clinical situations is required.Must have the ability to work collaboratively with other Ethicon team members to ensure open communication of ideas and techniques.   Must be highly organized and self-directed. Employee performance will be compared with other clinical specialists’ feedback provided accordingly.   Candidates must have a valid driver's license.As a salaried position, the hours are not restricted to “normal business hours” and ability to work flexible hours during days, nights and/or weekends as necessary is required.Travel is required as part of the position (approx. 75%).This position is bonus eligible, and the employee’s ability to meet the above requirements has a direct impact on this compensation.IQVIA offers a friendly, progressive work atmosphere and a comprehensive benefits package including medical, dental, life insurance and vision coverage, tuition assistance, bonus plan and 401(k). IQVIA is an EEO Employer - Minorities/Females/Protected Veterans/Disabled 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™. We look forward to the prospect of working with you! Please apply on-line at: www.IQVIA.com #LI-CES 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 $100-135,000 annually. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

Job Overview Secure and retain business through professional, consultative, proactive sales activities directed at decision-makers and decision influencers at existing and new pharmaceutical and healthcare clients. Support the growth of IQVIA’s Real World Evidence (RWE) business in LATAM, with focus on Colombia. This role is responsible for identifying and developing new business opportunities, managing client relationships, and partnering with internal teams to deliver tailored solutions that address client needs. The role operates within the regional RWE business and supports shared growth objectives in the market.  Essential Functions Actively prospect and leverage potential new business opportunities within existing and new customers/accounts.Build relationships with decision-makers and key stakeholders within pharmaceutical and healthcare organizations.Support the development and execution of account plans and sales plans for target customers.Lead and support sales discussions, client meetings, and presentations.Coordinate with internal scientific, technical, operational, contracts, and proposal teams to support proposal development and solution design.Manage follow-up activities related to proposals and sales opportunities.Maintain visibility within customer organizations and support customer satisfaction through regular communication.Monitor status of leads and opportunities to ensure an active and sustainable pipeline.Report sales activities and opportunities in CRM and provide updates to sales leadership as required.Serve as a liaison between the customer and IQVIA technical and operational teams.Qualifications Bachelor’s Degree in Business, Life Sciences, Pharmacy, Medicine, Public Health, or related discipline.Experience in business development, sales, account management, or related commercial roles within the pharmaceutical, CRO, healthcare, or consulting environment.Strong relationship-building and stakeholder management skills.Strong consultative selling, communication, and presentation skills.Strong business acumen and ability to identify and develop commercial opportunities.Strong organizational skills and ability to manage multiple priorities.Excellent English communication skills, written and verbal.Ability to work independently and effectively within cross-functional and multicultural teams.Preferred Qualifications Existing relationships with important pharmaceutical stakeholders in Colombia are a strong advantage.Experience working with scientific studies, evidence generation, or research-related solutions is preferred.Academic or professional background in scientific research is an advantage.Experience selling studies or research-based solutions is a strong differentiator.Experience in CROs, consulting firms, or pharmaceutical companies is preferred.Experience in pharmaceutical industry roles in business development, sales, research, or related areas is a plus.Familiarity with Real World Evidence, observational studies, database studies, or broader evidence-generation solutions is an advantage.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.

Buscamos una persona detallista para apoyar procesos de manejo de datos, incluyendo codificación y data bridging. Este rol es ideal para alguien con habilidades básicas en herramientas digitales, atención al detalle y motivación por trabajar con información y sistemas de datos. Serás responsable de transformar, validar y asegurar la calidad de los datos para que estén alineados con los sistemas de referencia de IQVIA. Responsabilidades principalesDesarrollar un entendimiento básico de procesos técnicos relacionados con codificación y vinculación (bridging) de datos Realizar procesos de codificación y mapeo de datos siguiendo lineamientos establecidos Convertir información de proveedores en formato físico a archivos electrónicos Interpretar información escrita y registrarla en sistemas internos de codificación Asegurar que los datos ingresados estén alineados con sistemas de referencia estándar Ejecutar controles de calidad para verificar la precisión de los datos ingresados Apoyar actividades de data bridging, comparando datos entrantes con bases de referencia de IQVIA Escalar problemas no rutinarios o complejos a miembros más experimentados del equipo RequisitosBachillerato completo o equivalente (requerido) Al menos 1 año de experiencia laboral usando herramientas de Office (Word y Excel) Conocimiento básico de procesos administrativos o técnicos Capacidad para seguir procedimientos establecidos y resolver tareas rutinarias Alta atención al detalle y precisión DeseableExperiencia en data entry, validación de datos o back office Conocimiento básico de bases de datos o sistemas de información Habilidades organizativas y manejo de tareas repetitivas 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.

As a global leader in commercial solutions, IQVIA is uniquely positioned to deliver results both nationally and internationally. Our teams partner with biopharma companies to bring essential medicines to the people who need them most. We empower our clients with insights and access to their markets, helping them demonstrate the value of their products to payers, physicians, and patients alike. A core part of our mission includes serving as the sales force for biopharma or providing nurse educators who support patients and prescribers. With the right experience, you can help bring medical innovations to life in real-world settings. We’re excited to announce an opportunity to join our team of over 10,000 field professionals worldwide—we’re currently hiring a Nurse Educator to support our pharmaceutical and biotech clients. Nurse Educator At the heart of our business strategies is a commitment to patients. The Nurse Educator Program is a patient-centered, educational initiative designed to support individuals living with chronic conditions who have been prescribed specific therapies. Nurse Educators play a vital role in helping patients understand their treatment, manage their condition, and access relevant resources related to their prescribed medication. This role involves one-on-one engagement with patients through various channels, including in-person visits, phone calls, video conferencing, email, and SMS—always in strict alignment with program guidelines. Please note: this is an educational role only. Nurse Educators do not provide clinical care or medical advice. Role Overview: Nurse Educator As a Nurse Educator, you will play a key role in supporting patients by connecting them with program-approved resources and delivering personalized education on chronic disease management and prescribed therapies. This role is designed to empower patients, promote treatment adherence, and encourage meaningful dialogue with healthcare providers. Key Responsibilities Facilitate connections between patients and approved educational resources. Deliver direct, disease-specific education and training related to prescribed medications. Support multiple disease states and therapies as needed. Promote behavioral change through patient-centered education to improve treatment adherence. Encourage effective communication between patients and their healthcare providers. Qualifications Bachelor’s degree and/or BSN preferred. Active RN license in state of residence; compact multi-state license preferred where applicable. Nursing license must be current and in good standing. Minimum of 5 years of clinical experience in healthcare (hospital, home health, pharmaceutical, or biotech settings). Prior experience as a nurse educator is preferred. Bilingual in English and Spanish is a plus. Valid driver’s license required. Must reside within the designated territory. Experience in direct patient interaction with a focus on adherence and persistence. Strong understanding of clinical data and pharmacology. Excellent time management, planning, and multitasking skills. Effective presentation and motivational skills; strong interpersonal and communication abilities. Ability to work independently and cross-functionally. Dedicated home workspace required. Adaptability to changing responsibilities and environments. Proficiency in Microsoft Office (Word, Excel, PowerPoint) and iPad technology. Flexibility to work evenings and weekends as needed. Willingness to travel up to 60–70%. Compliance with client vaccination requirements may be necessary. Compensation Competitive annual salary Car allowance Bonus eligibility  #LI-CES 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 $95,000-$105,000 annually. 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 88.000 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. Dazu gehören integrierte Projektansätze entlang unseres IQVIA-Lösungsportfolios, die wir individuell an Kundenbedürfnisse anpassen und aus einer Hand anbieten. Für einen bundesweiten Teamaufbau im Bereich Gynäkologie suchen wir zum 01.09.2026 mehrere Pharmaberater (m/w/d). Im Gebiet: Großraum Berlin Rollenbeschreibung Verantwortung für definierte gynäkologische Zielkunden und Aufbau nachhaltiger KundenbeziehungenUmsetzung des Markteintritts im Bereich Women’s Health auf GebietsebenePositionierung des Produkts sowie Durchführung fundierter FachgesprächeAufbereitung und Präsentation klinischer StudiendatenEntwicklung und Umsetzung individueller Account-PläneSteuerung der Gebietsperformance unter Nutzung von CRM-Tools (z. B. Veeva)Enge Zusammenarbeit mit internen Schnittstellen unter Einhaltung von Compliance-Vorgaben​Erforderliche Qualifikationen Ein abgeschlossenes Studium in Naturwissenschaften oder eine vergleichbare Qualifikation nach §75 AMGGültiger Führerschein sowie Reisebereitschaft innerhalb des jeweiligen GebietsErfahrung oder Kontakte im Bereich Gynäkologie / Women’s Health bevorzugtSicherer Umgang mit Compliance-Vorgaben (inkl. SAMs)Ausgeprägte Kundenorientierung und überzeugendes AuftretenSensibilität und Offenheit im Umgang mit Women’s Health ThemenErfahrung mit CRM-Systemen (z. B. Veeva) von VorteilGute Englischkenntnisse von VorteilDas 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 KrankenzusatzversicherungenEin top ausgestatteter Firmenwagen mit uneingeschränkter Privatnutzung (ohne Zuzahlung) und mit Wahlmöglichkeit des ModellsEine moderne IT-Ausstattung für Deinen modernen digitalen ArbeitsplatzUnser unbefristetes IQVIA Arbeitsverhältnis bietet Sicherheit und eine langfristige PerspektiveWir bieten u.a. tarifliche Sonderurlaubstage, Umzugszuschuss bei betrieblich bedingtem Wechsel deines WohnortsVielfältige 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 BeschäftigungsverhältnissesUnser 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 #PharmaceuticalSales #PharmaRepresentative #Pharmacy #FieldSales #Gynäkologie#Woman’s Health IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Job Overview Principal Data Manager position is to oversee data operations tasks for a team of data managers from study start-up to database lock, to produce a clean and analyzable database. Essential Functions • Serve as Data Team Lead (DTL) on a program of 6-10 global clinical trials or 40+ increasingly complex central laboratory studies• Provide leadership to CDM team.• Manage CDM customer relationship for CDM project team to include leading (with minimal guidance) CDM customer negotiations on complex timeline, budgetary and other issues.• Provide marketing capabilities presentations and business development presentations. . Or serve as Data Operations Coordinator (DOC) for one or three global clinical trials with fewer than 25 operations staff (excludes DE) or 20-40 central laboratory studies, or serve in a leadership role to a specific DM Task.• Serve as back-up for Data Operations Coordinator or Data Team Lead• Provide leadership to Operations team• Provide technical expertise. Or serve as a Subject Matter Expert (SME)• Provide leadership and expertise in a specific CDM task or technology. Manage delivery of projects through full data management process life-cycle.• Management of:• Project timelines• Quality issues• Resource management• SOW (scope of work) / budget. Provide justification for customer negotiations. May serve as Project Manager for single service data management projects. Manage comprehensive data management tasks pertaining to the documented project specifications. Manage comprehensive quality control procedures. Provide data management expertise and data management process improvement to CDM management. Mentor other team members in training and developing data management expertise. Independently bring project solutions to the CDM team and the CDM Department. Manage a focus team or a best practice team. Manage the development and implementation of new technology/tool. Present at professional conferences and/or publish articles in professional journals. Provide CDM with technical expertise. Provide review and expert opinion in developing, revising, and maintaining core operating procedures and working instructions. Perform other duties as directed by the functional manager. Meet objectives as assigned. Develop and maintain good communications and working relationships with CDM and project teams." Qualifications • Bachelor's Degree clinical, biological or mathematical sciences, or related field or nursing qualification Req• 5 years relevant experience including proven competence in managing delivery of multiple projects simultaneously through full data management study life-cycle, including large trials >1000 patients, and including experience handling customer negotiations (e.g. bid defense meetings). Equivalent combination of education, training and experience.• Thorough knowledge of the data management process and experience in specialized data management skills (e.g., therapeutic, extensive knowledge, SAE reconciliation, central laboratory, and/or new technology. Knowledge of operating procedures and work instructions and the ability to apply them in practice. Excellent experience and organizational, communication, and demonstrated expert data management skills. Comprehensive understanding of clinical drug development process (detail oriented). Ability to establish and maintain effective working relationships with coworkers, managers and clients. Thorough knowledge of the data management process and experience in specialized data management skills (e.g., therapeutic, extensive knowledge, SAE reconciliation, central laboratory, and/or new technology. Knowledge of operating procedures and work instructions and the ability to apply them in practice. Excellent experience and organizational, communication, and demonstrated expert data management skills. Comprehensive understanding of clinical drug development process (detail oriented). 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.

Internal Job DescriptionPURPOSE    Quality Reviewer      RESPONSIBILITIES    Conduct internal Data Management Quality Reviews in order to fulfil business unit, customer and regulatory authority requirements and expectations.Ensure that re-occurring findings/errors are communicated effectively with operational team.Participate in review of corrective/preventative actions.Assure recording of an appropriate response to any non-compliance, with corrective action and a timeframe for completion.Oversee the documentation and reporting quality/compliance issues, relating to the product, process or quality system, to Management within specified regional timelines.Collect and report quality metrics as required to Management.Maintain working knowledge of current applicable regulatory and Sponsor guidelines and related review techniques.Reviews aggregated information provided on the QRP and performs analysis and identification of trends on portfolio level.Reviews the error rate on study level and contact study teams where applicable to discuss CAPA.Liaise with Training Team to update training where needed. Independently bring solutions to the Quality Management Team Provide comprehensive quality review expertise Mentor junior Quality Review Staff REQUIRED KNOWLEDGE, SKILLS AND ABILITIES    Medical terminology exposure    Excellent organizational, communication, leadership and computer skills    Ability to exercise excellent attention to detail    Ability to act independently and with initiative required to resolving problems    Ability to establish and maintain effective working relationships with co-workers, managers and clients         MINIMUM REQUIRED EDUCATION AND EXPERIENCE      Bachelor’s degree, or educational equivalence, in clinical, biological or mathematical sciences, or related field, or nursing qualification with 5 years’ experience in clinical trials within a similar function, including proven competence in managing delivery of multiple projects simultaneously through full data management study life-cycle, including large trials >1000 patients; and including experience in handling customer negotiations (e.g. bid defence meetings); or equivalent combination of education, training and experience. 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 Description:1. Responsible for managing consulting/market research projects, including communicating with clients for debriefing and establishing project methodology;2. Responsible for the allocation of project resources, division of labor among the project team, and high quality delivery of reporting content;3. Responsible for the writing of pre-project proposals to help the team win the project;4. Responsible for the construction and analysis of data-related programs. Job responsibilities:1. Bachelor's or Master's degree； 2. At least 4 years in consulting or market research experience;3. Strong consulting/market research skills and project experience, as well as project management and client communication skills;4. Strong stress tolerance and problem solving skills. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Required skills and experience:• 4/5+ years of experience working with Azure and AWS or any other major cloud platform technologies• Provisioning, operating, and maintaining systems running on Azure and AWS cloud platforms including deployment/teardown with strong focus on automation and optimization• Proficient with cloud platforms including IaaS & PaaS components, for example: Azure Virtual Machines/EC2, Storage Accounts/S3, vNets/VPCs, Azure App Service/AWS Lambda, AKS/EKS, Azure SQL/RDS, messaging and integration services• Strong scripting and automation skills to reduce operational effort (PowerShell, Python, Bash, Azure CLI, AWS CLI)• Infrastructure as code (IaC), and CI/CD pipeline experience is required – example: Terraform, Bicep/ARM, CloudFormation, Gitlab, ADO• Expert level understanding of Windows and Linux operating systems from an administration perspective including system hardening, patching strategies, performance optimization, troubleshooting, capacity planning, and automation of OS-level tasks• Experience implementing monitoring and observability solutions (Azure Monitor, Log Analytics, Application Insights, CloudWatch, CloudTrail)• Experience managing backup, DR and patching across cloud platforms• Strong experience with security best practices including RBAC/IAM, encryption, logging and compliance controls• Strong knowledge of network (LAN, WAN, VPN) and web related protocols• Experience creating and maintaining operational documentation, runbooks and conducting knowledge transfer sessions• Excellent troubleshooting skills including complex OS, platform and cloud issues with root cause analysis• Experience with ITIL/ITSM processes including incident/request management, change and configuration management. Ideally ITIL Foundation certified. ServiceNow exposure is a bonus• Good awareness of latest Azure and AWS platform capabilities and ability to apply them in operations• Good to have: Understanding of AI for operations (AIOps, predictive monitoring, automation using AI, GenAI-based assistance tools)• Prior experience in Life Sciences area is also a bonus. Other highly regulated industry experience will be considered also Education/certification:•    Degree level educated, preferably in science, maths or engineering areas.•    Azure Certification is a must - preferably Azure Administrator or Solutions Architect certified. AWS certification (SysOps Administrator or Solutions Architect Associate) is preferred. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Required skills and experience:• 4/5+ years of experience working with Azure and AWS or any other major cloud platform technologies• Provisioning, operating, and maintaining systems running on Azure and AWS cloud platforms including deployment/teardown with strong focus on automation and optimization• Proficient with cloud platforms including IaaS & PaaS components, for example: Azure Virtual Machines/EC2, Storage Accounts/S3, vNets/VPCs, Azure App Service/AWS Lambda, AKS/EKS, Azure SQL/RDS, messaging and integration services• Strong scripting and automation skills to reduce operational effort (PowerShell, Python, Bash, Azure CLI, AWS CLI)• Infrastructure as code (IaC), and CI/CD pipeline experience is required – example: Terraform, Bicep/ARM, CloudFormation, Gitlab, ADO• Expert level understanding of Windows and Linux operating systems from an administration perspective including system hardening, patching strategies, performance optimization, troubleshooting, capacity planning, and automation of OS-level tasks• Experience implementing monitoring and observability solutions (Azure Monitor, Log Analytics, Application Insights, CloudWatch, CloudTrail)• Experience managing backup, DR and patching across cloud platforms• Strong experience with security best practices including RBAC/IAM, encryption, logging and compliance controls• Strong knowledge of network (LAN, WAN, VPN) and web related protocols• Experience creating and maintaining operational documentation, runbooks and conducting knowledge transfer sessions• Excellent troubleshooting skills including complex OS, platform and cloud issues with root cause analysis• Experience with ITIL/ITSM processes including incident/request management, change and configuration management. Ideally ITIL Foundation certified. ServiceNow exposure is a bonus• Good awareness of latest Azure and AWS platform capabilities and ability to apply them in operations• Good to have: Understanding of AI for operations (AIOps, predictive monitoring, automation using AI, GenAI-based assistance tools)• Prior experience in Life Sciences area is also a bonus. Other highly regulated industry experience will be considered also Education/certification:•    Degree level educated, preferably in science, maths or engineering areas.•    Azure Certification is a must - preferably Azure Administrator or Solutions Architect certified. AWS certification (SysOps Administrator or Solutions Architect Associate) is preferred. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Job OverviewResponsible for study build & design, edit specifications, system configurations and is accountable for associated study design components. This role will collaborate with various stakeholders- DTL, Programmer, Validation Team, vendors, statisticians, and client representatives. In addition to project deliveries, the role also would be responsible for the project financials from programming shared services perspective. Essential Functions• Interprets the study protocol.• Design and update the eCRF using third party or in house CDMS tools in alignment with industry standards like SDTM, CDASH as applicable.• Create and update Edit Specification Document.• Generate specifications for EDC build components (e.g., Rights and Roles, System Settings and Home Page)• Complete the Study Authorization Form and Trial Capacity Request Form (InForm)• Attend the Pre-Design Meeting, Online Screen Review Meeting, Unblinded Data review meeting.  Attend and present comments at the Internal Design Review Meeting.  May lead Online Screen Review Meeting.• Facilitate the internal Edit Specification Review Meeting and leads the discussions regarding the Edit Specification Document.• Design the database to collect LLRR data within the InForm database and ensure Rights and Roles document has appropriate access for Entry and Updates.• Communicate any project risks to the Data Team Lead, including the potential for missing a timeline in the Data Management Project Plan.• Escalate potential quality issues.• Ensure the completion and documentation of all project-specific training, as well as staying current with required Standard Operating Procedures.• Reviews build timelines and provide input as applicable.• Reviews QIP for own projects, identify out of scope activities if any and inform relevant parties.• Responsible for multiple study design projects at the same time.• Might be working on projects across multiple platforms.• Identify areas for process improvements on an ongoing basis. Actively take part and contribute towards process improvement initiatives as assigned besides providing suggestions for continuous improvement of processes.• All responsibilities are essential job functions unless noted as nonessential (N). Qualifications• Bachelor's Degree Bachelor in Science/Computer science/Information Technology or Bachelor in Technology  Req• 2-4 years of relevant core Technical designer experience and total exp being 7+ yrs.   Req IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

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