Senior Epidemiologist, Immunology, RWE (FSP Sponsor Dedicated)

Location: Remote candidates should preferably be based in Spain Portugal or UK (other EU locations may be considered).

Join IQVIAs 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 this role youll work closely with one sponsor gaining deep knowledge of their therapies while leveraging IQVIAs global expertise.

Core Function Description:

This role will support the Inflammation Real World Evidence team providing scientific and strategic epidemiology support for clinical development and drug safety activities. This role will leverage secondary real-world data (RWD) sources to generate evidence that informs regulatory safety and clinical development decisions across the product lifecycle.

Key responsibilities include designing and conducting observational research studies assessing evidence gaps evaluating safety profiles and developing evidence strategies to support regulatory interactions and clinical development programs. The Senior Epidemiologist will collaborate closely with cross-functional teams including Clinical Development Safety Regulatory Affairs Biostatistics and Real-World Evidence stakeholders to ensure appropriate epidemiologic approaches are applied to address critical business and scientific questions.

The ideal candidate will have deep expertise in epidemiologic methods demonstrated experience working within pharma or biotech and a thorough understanding of regulatory requirements related to clinical development and safety evidence generation.

This is a fully remote position based in the United States.

Minimum Qualifications

• Doctoral degree (PhD ScD or equivalent) in Epidemiology.

• 5 to 7 years of epidemiology experience within apharmaceutical/biotechnologycompany.

• Demonstrated experience supporting clinical development and/or drug safety.

• Strong expertise in observational research methods and the use of commercial healthcare databases such as HealthVerity Pharmetrics Plus TriNetX or similar real-world data assets.

• Solid understanding of regulatory requirements and evidence needs supporting clinical development including the generation of evidence to address regulatory questions related to safety profiles and evidence gaps for Phase II and Phase III programs.

• Proven ability to design execute and interpret epidemiologic studies that support regulatory clinical or safety objectives.

Preferred Qualifications

• Experience in Inflammation and Immunology therapeutic areas.

• Knowledge of disease areas such as Atopic Dermatitis Asthma Lupus Immune Thrombocytopenia (ITP) Autoimmune Hemolytic Anemia or other immune-mediated diseases.

• Experience supporting assets within emerging immunology programs.

• Experience working with primary or hybrid real-world data sources in addition to secondary data sources.

• Prior experience supporting regulatory submissions or interactions with FDA EMA or other global health authorities.

Whats in it for you

• 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 IQVIAs 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

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 Experience:

Senior IC

Employment Type : Full-Time
Experience: years
Vacancy: 1