Lisbon, Portugal · Remote OK
Principal Epidemiologist, Internal Medicine, Inflammation & Immunology (FSP Sponsor Dedicated) Location: Remote, candidates should preferably be based in Spain, Portugal or UK (other EU locations may be considered). Join…
Skills: Literature Review, Data Cleaning, Quality Control, Scientific Writing, Epidemiologic Methods
Tokyo, Japan · On-site
◆Hiring Managerからのメッセージ 本ポジションは、契約管理の中核を担いながら、将来的にチームをリードいただくことを期待するリーダー候補のポジションです。 当社はヘルスケア領域において、医療の発展や社会課題の解決に貢献しており、本ポジションも契約業務を通じて事業の推進を支える重要な役割を担います。営業やコンサルティング部門、法務や財務部門と密に連携し、ビジネスの円滑な推進に直接関わることができます。 現在は、業務の標準化や効…
Skills: Contract Drafting, Contract Review, Corporate Legal Affairs, Stakeholder Management, Japanese Language Proficiency
Bucharest, Romania · Remote OK
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 D…
Skills: Clinical Data Management, Study Setup, Database Lock, Data Reconciliation, Resource Allocation
Taguig, Metro Manila, Philippines · On-site
Title: Sr Prod Data Input Assoc GRE120 Role Purpose: Under guidance maintains more complex reference files needed by IQVIA production. Principal Accountabilities: This position will support the current Outlet Reference t…
Skills: Microsoft Excel, Microsoft Access, SQL, Relational Databases, Data Maintenance
Greenwich, Connecticut, United States · Hybrid
$93k–$232k/yr
About Cedar Gate Technologies Cedar Gate Technologies, an IQVIA business, enables payers, providers, employers, and service administrators to excel at value-based care with a unified technology and services platform deli…
Skills: .NET, Java, AWS, Azure, Microservices
Amsterdam, North Holland, Netherlands · Remote OK
IQVIA™ is the leading human data science company focused on helping healthcare clients find unparalleled insights and better solutions for patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a b…
Skills: Site Monitoring, Good Clinical Practice (GCP), ICH Guidelines, Subject Recruitment, Medical Writing
Amsterdam, North Holland, Netherlands · Remote OK
IQVIA™ is the leading human data science company focused on helping healthcare clients find unparalleled insights and better solutions for patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a b…
Skills: Site Monitoring, GCP, ICH Guidelines, Subject Recruitment, Medical Writing
Amsterdam, North Holland, Netherlands · Remote OK
IQVIA™ is the leading human data science company focused on helping healthcare clients find unparalleled insights and better solutions for patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a b…
Skills: Site Monitoring, Good Clinical Practice (GCP), ICH Guidelines, Subject Recruitment, Medical Writing
Beijing, Beijing, China · On-site
Provide support to management in the promotion and assessment of compliance with regulations, guidelines, and operating procedures. Manage the quality assurance oversight of projects, assignments, training and staff. Con…
Skills: GXP Regulations, Quality Assurance, Auditing, Risk Analysis, Leadership
Remote Solely
Exciting Opportunity for Freelance Medical Post-Editors English-Irish! Do you have a keen eye for detail and a passion for ensuring the accuracy and clarity of medical documents? We’re on the hunt for skilled Freelance M…
Skills: Medical Post-Editing, Clinical Translation, English-Irish Translation, Clinical Terminology, Medical Writing
Buenos Aires, Argentina · On-site
Job Overview The Specimen Receipt and Processing Associate is responsible for assisting with a variety of routine activities associated with receipt of clinical specimens. Essential Functions • Responsible for assisting …
Skills: Specimen Receipt, Quality Control, Inventory Management, Administrative Support, Computer Skills
Bratislava, Region of Bratislava, Slovakia · On-site
$19k–$28k/yr
Financial Analyst – Business Operations Support About the Role This role sits within the Global Procurement and Travel & Payment Solutions team and acts as a hybrid between Finance, Operations, and Customer Support. The …
Skills: Financial Postings, Reconciliations, Journal Entries, Data Analysis, Process Automation
London, England, United Kingdom · Hybrid
Type: Permanent full time Location: London Schedule: Monday – Friday, 9-5 (with some flexibility) We are looking for an experienced registered nurse to join the team in the London area. In this fantastic role, you will b…
Skills: Phlebotomy, Cannulation, Infusion, Caseload Management, IT Skills
Warsaw, Masovian Voivodeship, Poland · Hybrid
$180k–$264k/yr
Are you a technically strong Digital Project Manager with a passion for building scalable platforms and leading end-to-end delivery? We’re looking for someone who can combine product thinking, technical leadership, and h…
Skills: Digital Project Management, Drupal, PHP, Microsoft Azure, Acquia
Prague, Prague, Czechia · On-site
Essential Functions Develop Coordinate the development of investigator grants and estimates, contracting strategies and proposal text to support the proposal development process.Develop contract language, payment languag…
Skills: Contract Negotiation, Budget Development, Clinical Site Contracting, Legal Writing, Financial Analysis
Chengdu, Sichuan, China · On-site
Essential Functions Manage about 1 local Prime site，6 other strategic sites which may locate in the other cities. Works under moderate supervision to develop new alliance site and maintain the cooperation. Support implem…
Skills: Site Management, Clinical Research, Patient Recruitment, Stakeholder Management, Strategic Planning
Illkirch-Graffenstaden, Grand Est, France · On-site
Job Overview Manage 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. Support senior leadership on re…
Skills: Clinical Trial Management, People Management, Resource Allocation, GCP, ICH Guidelines
Chicago, Illinois, United States · On-site
$169k–$470k/yr
Join us on our exciting journey! IQVIA™ is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients. Formed through the merger of IMS Health a…
Skills: Consultative Selling, Strategic Account Management, Pharma Commercial Strategy, Stakeholder Management, Cross-functional Leadership
Berchem, Flanders, Belgium · On-site
Site Enrollment and Engagement Leads collaborate with research staff and other stakeholders to drive trial recruitment and support study-specific training needs. The role acts as a strategic partner to both external and …
Skills: Trial Recruitment, Relationship Management, Clinical Trial Protocols, Patient Pre-screening, Stakeholder Management
Athens, Attica, Greece · Hybrid
Team IQVIA is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. IQVIA creates intelligent connections across all aspects of healthcare th…
Skills: Systematic Literature Review, Health Economics Outcomes Research, Database Searching, OVID SP, PRISMA Principles
Lisbon, Portugal • Remote OK
Sign up with Clera and we'll reach out the moment a role actually fits you — no more spraying applications into the void.
Provide scientific support for RWE/Epidemiology studies through literature reviews, data cleaning, and the development of scientific deliverables. Coordinate operational activities and oversee vendor deliverables to ensure high-quality study execution.
Requires a Master's degree (MPH minimum) with a PhD in Epidemiology preferred. Candidates should have experience in applied epidemiology or scientific operations, particularly within chronic disease therapeutic areas.
Location: Remote, candidates should preferably be based in Spain, Portugal or UK (other EU locations may be considered).
Join IQVIA’s Sponsor-Dedicated FSP team and help advance healthcare through real-world evidence. We bring together scientific expertise and real-world data to help sponsors make decisions and accelerate evidence generation to improve patient outcomes.
In this role, you’ll work closely with one sponsor, gaining deep knowledge of their therapies while leveraging IQVIA’s global expertise.
Overview:
This role provides scientific and strategic leadership for RWE/Epidemiology studies, serving as the primary lead for assigned studies or scientific workstreams, accountable for ensuring the scientific rigor and operational feasibility of studies in alignment with Medical Evidence Generation priorities.
This role provides scientific expertise to drive high-complexity deliverables such as protocols, publications, and analyses that meet the Pfizer quality standards.
This role may represent Pfizer in scientific discussions with vendors and external stakeholders.
Organizational Relationships:
Reports to the sponsor’s RWE/Epidemiology Lead within their Integrated Evidence Generation (IEG) organization
Collaborates with Medical Evidence Development (MED) colleagues, CMO colleagues (e.g., DS&A, Regulatory, Safety), Clinicians, HV&E/GAV, and other cross-functional scientific partners to drive study design and execution
Interfaces with other external vendors supporting study design and execution
Scientific Expertise:
Serves as a subject matter expert in epidemiology or related field
Provides strategic guidance on scientific approach and analytical methodologies
Leads development of scientific deliverables (e.g., study concepts, study protocols, statistical analysis plan, etc.)
Ensures quality and scientific integrity across all outputs
Conducts and oversees literature reviews
Support real world data assessment and landscape evaluation, especially for new data sets and networks in Europe
Responds to rapid epidemiological requests, including safety questions and information requests
Study Execution Oversight:
Provides input on study feasibility and resource needs
Leads scientific oversight of study execution, in collaboration with MED Evidence Generation Ops teams and external vendors
Ensures quality review and contributes to inspection/audit readiness for RWE/Epi studies
Performs/oversees code lookup and data QC tasks to ensure inclusivity and avoid assumptions about task ownership
Performs other relevant tasks as needed to support study execution
Requirements:
Training and Education Preferred:
PhD in Epidemiology or related field
Or in rare exceptions Master’s with significant experience
Prior Experience Preferred:
Experience designing and/or leading RWE/Epidemiology studies
Good knowledge and hands-on experience in the field of migraine, obesity or anti-infectives is preferred, but is not essential
Experience designing study protocols, research reports, and/or publications
Experience working in a matrixed, cross-functional team environment
Experience in the fields of chronic diseases such as: inflammation, immunology, rare disease, anti-infectives, migraine/obesity, CV/metabolic. Migraine/obesity experience is advantageous but not essential.
Skills:
Deep expertise in epidemiologic methods
Strong verbal and written communication skills
Strong organizational skills and project management capability
Ability to work effectively in a cross-functional environment and operate as a team player
Ability to collaborate with analysts/programmers to ensure execution of analysis plans
Be part of a forward-thinking team that helps shape the next generation of evidence-based healthcare.
Work hand-in-hand with one leading sponsor, gaining deep expertise in their therapies.
Access IQVIA’s global network who supports your growth
This is your chance to make an impact, while building a career that matters.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
IQVIA (NYSE:IQV) is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. IQVIA’s portfolio of solutions are powered by IQVIA Connected Intelligence™ to deliver actionable insights and services built on high-quality health data, Healthcare-grade AI™, advanced analytics, the latest technologies and extensive domain expertise. With approximately 88,000 employees in over 100 countries, including experts in healthcare, life sciences, data science, technology and operational excellence, IQVIA is dedicated to accelerating the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. IQVIA is a global leader in protecting individual patient privacy. The company uses a wide variety of privacy-enhancing technologies and safeguards to protect individual privacy while generating and analyzing information on a scale that helps healthcare stakeholders identify disease patterns and correlate with the precise treatment path and therapy needed for better outcomes. IQVIA’s insights and execution capabilities help biotech, medical device and pharmaceutical companies, medical researchers, government agencies, payers and other healthcare stakeholders tap into a deeper understanding of diseases, human behaviors and scientific progress, in an effort to advance healthcare. To learn more, visit www.iqvia.com.
Offices: 2400 Ellis Rd, Durham, North Carolina 27703, US
IQVIA (NYSE:IQV) is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. IQVIA’s portfolio of solutions are powered by IQVIA Connected Intelligence™ to deliver actionable insights and services built on high-quality health data, Healthcare-grade AI™, advanced analytics, the latest technologies and extensive domain expertise. With approximately 88,000 employees in over 100 countries, including experts in healthcare, life sciences, data science, technology and operational excellence, IQVIA is dedicated to accelerating the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. IQVIA is a global leader in protecting individual patient privacy. The company uses a wide variety of privacy-enhancing technologies and safeguards to protect individual privacy while generating and analyzing information on a scale that helps healthcare stakeholders identify disease patterns and correlate with the precise treatment path and therapy needed for better outcomes. IQVIA’s insights and execution capabilities help biotech, medical device and pharmaceutical companies, medical researchers, government agencies, payers and other healthcare stakeholders tap into a deeper understanding of diseases, human behaviors and scientific progress, in an effort to advance healthcare. To learn more, visit www.iqvia.com.
Offices: 2400 Ellis Rd, Durham, North Carolina 27703, US
