Senior Research Scientist, Pharmacoepidemiology/Safety

This is a fully remote position, open to applicants in France, +4 more countries.

📋 Description

• Design and implement Epidemiology studies that focus on safety research inquiries.

• Identify appropriate epidemiological and pharmaco-epidemiological methodologies, relevant data sources that are best suited to address safety research inquiries.

• Conduct feasibility assessments, design study concepts, prepare protocols, statistical analysis plans, and reports for pharmacoepidemiologic studies.

• Transfer epidemiological expertise and deliverables to enhance the evaluation, refinement, and contextualization of safety findings.

• Employ analytical techniques to interpret real-world data, assisting in identifying safety data gaps to generate valuable insights.

• Contribute to the development of Integrated Evidence Generation Plans (IEGPs), which include planning, prioritization, and execution of real-world studies, particularly focusing on safety aspects and outcomes.

• Communicate safety-related real-world data (RWD) internally and externally in a timely manner to all relevant stakeholders.

• Collaborate with Scientific Communications to create integrated publication plans for safety evidence.

• Promote a culture of continuous learning and improvement.

⛳️ Requirements

• A background in health and life sciences (epidemiology, public health, MD, PharmD), or quantitative data sciences, biostatistics.

• A PhD in Epidemiology and/or pharmacoepidemiology or equivalent is advantageous.

• Over 12 years of experience in epidemiology/pharmacoepidemiology and drug safety.

• Exceptional written and oral communication skills in English.

• Strong medical and scientific background, motivated by a commitment to patient safety.

• Solid working knowledge of both Good Clinical Practice (GCP) and Good Vigilance Practice (GVP).

• Significant prior experience working with Real-World Evidence (RWE) within the pharmaceutical industry, especially in the application of RWE in drug development for rare indications is a plus.

• Willingness to travel up to 20% of the time as required.

🏝️ Benefits

• Competitive salary

• Flexible working hours

• Professional development opportunities