Pharmacoepidemiologist M/F

JR France; Angoulême; Sur place; EUR 50 000 - 70 000; Plein temps

Résumé du poste

Join a leading Contract Research Organization as a Pharmacoepidemiologist. Contribute to impactful clinical research by ensuring scientific quality and managing studies. Ideal candidates possess a Master's degree or higher, with at least 5 years of relevant experience. Opportunities for career growth in a diverse and inclusive environment await you.

Prestations

Career development opportunities

Supportive environment

Diversity, Equality, and Inclusion initiatives

Qualifications

• At least 5 years of experience in a similar role.
• Ability to manage projects and work across multidisciplinary teams.

Responsabilités

• Ensuring scientific quality of studies and managing operational follow-up.
• Conducting epidemiological evaluation of safety signals.
• Writing summaries for regulatory authorities.

Connaissances

Project Management

Listening Skills

Diplomacy

Epidemiology

Public Health

Formation

Master's degree (BAC+5)

PhD

PharmD

Description du poste

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Join Aixial Group as a Pharmacoepidemiologist (M/F)

Are you a highly skilled professional passionate about life sciences and clinical research? Do you thrive in a dynamic, collaborative international environment where your expertise impacts people's lives? Come and contribute to shaping the future of clinical research with Aixial Group!

We are looking for a Pharmacoepidemiologist (M/F) to perform the following (non-exhaustive) tasks:

1. Ensuring the scientific quality of entrusted studies (protocols, statistical analysis plans, study reports, result interpretation, study documents, project meetings)
2. Managing the operational follow-up of studies (management of service providers, internal procedures related to studies)
3. Conducting epidemiological evaluation of safety signals (literature review and analysis)
4. Contributing to updates of crisis management plans, responding to health authority queries, and participating in cross-functional meetings (with pharmacovigilance, medical affairs, regulatory affairs)
5. Writing summaries for regulatory authorities in a confidential context
6. Following operational procedures while respecting deadlines
7. Analyzing pharmacoepidemiological literature for safety signals/SER, RMP, PBRER/PSUR
8. Reviewing protocols, statistical analysis plans, and study reports for PASS (Post-Authorization Safety Study)
9. Ensuring timely submission of PASS study documents to regulatory authorities

Your profile:

• Master's degree (BAC+5), PhD, PharmD, or equivalent in public health, epidemiology
• At least 5 years of experience in a similar role
• Ability to manage projects and work across multidisciplinary teams: medical, regulatory, marketing, etc.
• Good listening skills and diplomacy
• Fluent in English (written and spoken)
• Professional or fluent level in French is a plus

About us:

• We are one of the world’s leading CROs (Contract Research Organization), committed to delivering efficient clinical trials through expertise and flexibility.
• We collaborate with global pharmaceutical, biotech, cosmetic, medical device companies, among others, providing innovative, scalable solutions.
• Operating in 10 countries across 3 continents, with over 1000 talented professionals dedicated to making a positive impact in life sciences.
• Part of ALTEN Group since 2014, continuously expanding our global activities.

Why join us?

• Make a positive impact by being part of groundbreaking clinical research that benefits millions worldwide.
• Enjoy career development opportunities in a supportive environment that fosters growth, flexibility, and teamwork, with coaching and mentoring.
• We value Diversity, Equality, and Inclusion, promoting dignity, respect, and recognizing individual differences. Gender equality is central to our strategy.

Aixial Group continues to grow and recruit in clinical trial professions. Join us and follow our latest news and offers on our website.