Pharmacoepidemiologist M/F

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

Résumé du poste

Join a leading global CRO as a Pharmacoepidemiologist, where you'll ensure scientific quality and evaluate safety signals in clinical research. Contribute to impactful studies while working in a dynamic, collaborative environment. Your expertise will shape the future of clinical trials, and you'll have opportunities for career development and growth.

Prestations

Career development with coaching

Commitment to Diversity, Equality, and Inclusion

Qualifications

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

Responsabilités

• Ensuring scientific quality of studies and operational follow-up.
• Evaluating safety signals epidemiologically and writing summaries for authorities.
• Analyzing scientific literature related to safety signals.

Connaissances

Project Management

Diplomacy

Listening Skills

Formation

Master’s degree in public health

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 contribute to shaping the future of clinical research!

We are seeking a Pharmacoepidemiologist (M/F) to perform the following key responsibilities:

1. Ensuring scientific quality of studies (protocols, statistical analysis plans, reports, interpretation, documents, meetings)
2. Operational follow-up of studies (managing service providers, internal procedures)
3. Evaluating safety signals epidemiologically (literature review and analysis)
4. Updating crisis management plans, responding to health authority queries, and participating in cross-functional meetings (with pharmacovigilance, medical, regulatory teams)
5. Writing summaries for regulatory authorities in a confidential context
6. Following operational procedures and respecting deadlines
7. Analyzing scientific literature related to safety signals/SER, RMP, PBRER/PSUR
8. Reviewing protocols, analysis plans, and study reports for PASS
9. Ensuring timely submission of PASS 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 experience in a similar role
3. Ability to manage projects and work across multidisciplinary teams
4. Good listening skills and diplomacy
5. Fluent in English (spoken and written)
6. Professional or fluent level in French is a plus

Who are we?

• Global leader in CRO (Contract Research Organization), delivering efficient clinical trials with expertise and flexibility
• Partnering with pharmaceutical, biotech, cosmetic, medical device companies worldwide, offering innovative solutions
• Operating in 10 countries across 3 continents with over 1000 professionals committed to positive impact in life sciences
• Part of ALTEN Group since 2014, continually expanding worldwide

Why join us?

• Make a positive impact through groundbreaking clinical research affecting millions globally
• Career development with coaching and mentoring to support your growth
• Commitment to Diversity, Equality, and Inclusion, promoting dignity, respect, and gender equality

Aixial Group continues to grow and recruit in clinical trial professions. Join us and visit our website for the latest news and offers.