Pharmacoepidemiologist M/F

JR France; Arras; Sur place; EUR 50 000 - 75 000; Plein temps

Résumé du poste

A leading global CRO is seeking a Pharmacoepidemiologist to ensure the scientific quality of studies and manage operational follow-up. Ideal candidates will have a Master's degree or higher, with at least 5 years of experience. Join a dynamic team impacting clinical research globally.

Prestations

Career development with coaching and mentorship

Commitment to diversity, equality, and inclusion

Qualifications

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

Responsabilités

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

Connaissances

Project management

Good listening skills

Diplomacy

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 want to thrive in a dynamic, collaborative international environment where your expertise impacts 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 scientific quality of studies (protocols, statistical analysis plans, reports, interpretation, documents, 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, respond to health authority queries, participate in cross-functional meetings (pharmacovigilance, medical affairs, regulatory affairs)
5. Write summaries for regulatory authorities in a confidential context
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
9. Ensure timely submission of PASS study documents to 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. Project management skills and ability to work across multidisciplinary teams
4. Good listening skills and diplomacy
5. Fluent in English (spoken and written)
6. Professional or fluent French skills are a plus

Who are we?

• Leading global CRO, committed to delivering efficient clinical trials
• Work with pharmaceutical, biotech, cosmetic, medical device companies worldwide
• Operate in 10 countries across 3 continents with over 1000 professionals
• Part of ALTEN Group since 2014, expanding globally

Why join us?

• Make a positive impact on millions through groundbreaking clinical research
• Career development with coaching and mentorship
• Commitment to diversity, equality, and inclusion, promoting dignity and respect

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