Pharmacoepidemiologist M/F

JR France; Saint-Herblain; Sur place; EUR 60 000 - 80 000; Plein temps

Résumé du poste

A leading global CRO is seeking a Pharmacoepidemiologist to ensure scientific quality in clinical research. The role involves managing studies, analyzing safety signals, and writing regulatory summaries. Join a dynamic team dedicated to impactful research and career growth.

Prestations

Career development opportunities

Coaching and mentoring

Commitment to Diversity, Equality, and Inclusion

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 operational follow-up.
• Managing epidemiological evaluation of safety signals.
• Writing summaries for regulatory authorities.

Connaissances

Project Management

Listening Skills

Diplomacy

Epidemiology

Public Health

Fluency in English

Fluency in French

Formation

Master's degree (BAC+5)

PhD

PharmD

Description du poste

Social network you want to login/join with:

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Client:

AIXIAL GROUP

Location:

saint-herblain, France

Job Category:

Other

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EU work permit required:

Yes

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Job Reference:

3403990886088966144327663

Job Views:

3

Posted:

15.05.2025

Expiry Date:

29.06.2025

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Job Description:

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

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

• Ensuring scientific quality of studies (protocols, analysis plans, reports, etc.)
• Operational follow-up of studies (management of service providers, internal procedures)
• Managing epidemiological evaluation of safety signals (literature review and analysis)
• Contributing to crisis management updates, health authority responses, and participating in cross-functional meetings (pharmacovigilance, medical, regulatory)
• Writing summaries for regulatory authorities in a confidential context
• Following operational procedures while respecting deadlines
• Analyzing pharmacoepidemiological literature for safety signals/SER, RMP, PBRER/PSUR
• Reviewing protocols, analysis plans, and study reports for PASS
• Ensuring timely submission of PASS documents to authorities

Your profile:

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

About us:

• We are a global leader in CRO (Contract Research Organization) with expertise and flexibility in clinical trials.
• We collaborate with pharmaceutical, biotech, cosmetic, medical device companies worldwide, offering innovative solutions.
• Operating in 10 countries across 3 continents with over 1000 professionals
• Part of ALTEN Group since 2014, continuously expanding globally.

Why join us?

• Make a positive impact by participating in groundbreaking clinical research benefiting millions worldwide.
• Career development with coaching, mentoring, and growth opportunities.
• Dedicated to Diversity, Equality, and Inclusion, promoting respect and recognizing individual differences.

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