Pharmacoepidemiologist M/F

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

Résumé du poste

Join a leading CRO as a Pharmacoepidemiologist in Cannes, where you'll ensure the scientific quality of studies and manage safety evaluations. This role offers the chance to impact lives through clinical research in a collaborative environment.

Prestations

Career Development Opportunities

Supportive Environment

Commitment to Diversity, Equality, and Inclusion

Qualifications

• Minimum of 5 years of experience in a similar role.
• Fluent in English, professional level in French is a plus.

Responsabilités

• Ensure the scientific quality of entrusted studies.
• Oversee operational follow-up of studies.
• Manage epidemiological evaluation of safety signals.

Connaissances

Project Management

Diplomacy

Listening Skills

Formation

Master's degree in public health

PhD in epidemiology

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 can impact lives? Join Aixial Group and help shape the future of clinical research!

We are seeking a Pharmacoepidemiologist (M/F) to perform the following responsibilities (non-exhaustive list):

1. Ensure the scientific quality of entrusted studies (protocols, statistical analysis plans, study reports, result interpretation, study documents, project meetings).
2. Oversee operational follow-up of studies (management of service providers, internal procedures related to studies).
3. Manage epidemiological evaluation of safety signals (literature review and analysis).
4. Contribute to updates of crisis management plans, respond to health authority queries, and participate in cross-functional meetings (with pharmacovigilance, medical affairs, regulatory affairs).
5. Write summaries for regulatory authorities in a confidential context.
6. Follow operational procedures while respecting deadlines.
7. Analyze pharmacoepidemiological literature for safety signals/SER, RMP, PBRER/PSUR.
8. Review protocols, statistical analysis plans, and study reports for PASS.
9. Ensure timely submission of PASS study documents to regulatory authorities.

Your profile:

1. Master's degree (BAC+5), PhD, PharmD in public health, epidemiology, or equivalent.
2. Minimum of 5 years of experience in a similar role.
3. Ability to manage projects and work transversally across multidisciplinary teams.
4. Good listening skills and diplomacy.
5. Fluent in English (written and spoken).
6. Professional or fluent level in French is a plus.

Who Are We?

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

Why Join Us?

• Make a positive impact by contributing to groundbreaking clinical research affecting millions worldwide.
• Enjoy career development opportunities in a supportive environment that fosters growth, flexibility, and teamwork.
• Be part of a company committed to Diversity, Equality, and Inclusion, promoting dignity and respect for all employees.

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