Pharmacoepidemiologist M/F

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

Résumé du poste

A leading company in clinical research is seeking a Pharmacoepidemiologist to ensure scientific quality and manage operational follow-up of studies. The ideal candidate will have a Master's degree or higher in a relevant field and at least 5 years of experience. Join a collaborative international team making a positive impact in life sciences.

Prestations

Career development opportunities

Diversity, Equality, and Inclusion commitment

Qualifications

• Minimum of 5 years of relevant experience.
• Master's degree (BAC+5), PhD, PharmD in public health, epidemiology, or related field.

Responsabilités

• Ensure scientific quality of studies including protocols and reports.
• Manage operational follow-up of studies and service providers.
• Conduct epidemiological evaluation of safety signals.

Connaissances

Project Management

Listening Skills

Diplomacy

Fluent in English

Fluent in French

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 impacts lives? Come 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 scientific quality of studies including protocols, statistical analysis plans, study reports, and result interpretation.
2. Manage operational follow-up of studies, including oversight of service providers and adherence to internal procedures.
3. Conduct epidemiological evaluation of safety signals through literature review and analysis.
4. Contribute to crisis management updates, health authority responses, and participate in cross-functional meetings with pharmacovigilance, medical, and regulatory teams.
5. Write confidential summaries for regulatory authorities.
6. Follow operational procedures carefully, respecting deadlines.
7. Analyze pharmacoepidemiological literature for safety signals, SER, RMP, PBRER/PSUR.
8. Review protocols, analysis plans, and study reports for PASS (Post-Authorization Safety Studies).
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 related field.
2. Minimum of 5 years of relevant experience.
3. Ability to manage projects and work 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?

1. We are a world leader in CRO (Contract Research Organization), committed to delivering efficient clinical trials.
2. We collaborate with global pharmaceutical, biotech, cosmetic, medical device, and other companies, providing innovative solutions.
3. Operating in 10 countries across 3 continents with over 1000 professionals dedicated to making a positive impact in life sciences.
4. Part of ALTEN Group since 2014, continuously expanding our global presence.

Why join us?

1. Make a positive impact by advancing clinical research that benefits millions worldwide.
2. Enjoy career development opportunities in a supportive, growth-oriented environment.
3. We are committed to Diversity, Equality, and Inclusion, fostering a respectful workplace where individual differences are valued and gender equality is prioritized.

Aixial Group is growing and recruiting in clinical trial professions. Join us and follow our news and offers on our website.