Pharmacoepidemiologist M/F

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

Résumé du poste

Join a leading CRO as a Pharmacoepidemiologist in Marseille, where you'll ensure the scientific quality of studies and manage operational follow-up. This role offers impactful work that benefits millions globally, with a focus on career development and diversity.

Prestations

Career development with coaching and mentorship

Commitment to diversity, equality, and inclusion

Qualifications

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

Responsabilités

• Ensure scientific quality of studies and manage operational follow-up.
• Evaluate safety signals epidemiologically and write summaries for regulatory authorities.

Connaissances

Project management

Listening skills

Diplomatic skills

Formation

Master's degree

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 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:

1. Ensure scientific quality of studies (protocols, statistical analysis plans, reports, result interpretation, documentation, meetings)
2. Manage operational follow-up of studies (service providers, internal procedures)
3. Evaluate safety signals epidemiologically (literature review and analysis)
4. Contribute to crisis management updates, health authority responses, and cross-functional meetings (pharmacovigilance, medical, regulatory)
5. Write summaries for regulatory authorities in a confidential context
6. Follow operational procedures while respecting deadlines
7. Analyze scientific literature for safety signals, RMP, PBRER/PSUR
8. Review protocols, analysis plans, and study reports for PASS (Post-Authorization Safety Study)
9. Ensure timely submission of PASS documents to authorities

Your profile:

1. Master's degree (BAC+5), PhD, PharmD in public health, epidemiology or related field
2. Minimum of 5 years experience in a similar role
3. Project management and ability to work across multidisciplinary teams
4. Good listening and diplomatic skills
5. Fluent in English (written and spoken)
6. Professional or fluent in French is a plus

About Us:

• Leading CRO with expertise and flexibility for efficient clinical trials
• Partner to global pharmaceutical, biotech, cosmetic, medical device companies
• Operating in 10 countries across 3 continents with over 1000 professionals
• Part of ALTEN Group since 2014, expanding worldwide

Why Join Us?

• Impactful work that benefits millions globally
• Career development with coaching and mentorship
• Commitment to diversity, equality, and inclusion, promoting respect and valuing differences

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