This role is based in the Barcelona, Spain office, with a minimum in‑office requirement of two days per week.

What You’ll Do

We are looking for someone with a strong combination of skills and experience in pharmacoepidemiology, risk management, and other regulatory‑grade real‑world evidence (RWE) research, along with the ability to work effectively in a collaborative, multidisciplinary research environment.

In this role, you will contribute to, or co‑lead, field and database regulatory‑grade studies on the use, safety, and effectiveness of treatments and prevention across a range of therapeutic areas. This includes supporting pre‑ and post‑approval regulatory applications of RWE, such as external control arms and label extensions.

To be successful in this role, you will possess:

• Demonstrated effective communication skills (written, verbal, presentation) in a cross‑functional, collaborative environment.
• Ability to e...