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Regulatory Affairs Pharmacist – France

0-2 years
Not Disclosed
10 May 1, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Regulatory Affairs Pharmacist – France
Slug: regulatory-affairs-pharmacist-france-excelya

Position: Regulatory Affairs Pharmacist
Type: Full-time, Permanent
Location: France
Company: Excelya


Why Join Excelya:
Excelya is a growing healthcare company with a team of 900+ professionals ("Excelyates") committed to delivering excellence in clinical research. Our unique one-stop service model—spanning full-service CRO, functional service provision, and expert consulting—offers a collaborative environment that nurtures scientific innovation, teamwork, and individual growth. We are driven to become Europe’s leading mid-size CRO while ensuring the best employee experience.


About the Role:
As a Regulatory Affairs Pharmacist, you will be part of a dynamic Regulatory Affairs team and contribute to shaping the future of healthcare by ensuring compliance with national and European regulatory standards. This is a key role in supporting promotional, packaging, and registration activities—impacting both market access and patient safety. The position offers a stimulating environment where bold ideas, collaboration, and continuous development are encouraged.


Key Responsibilities:

  • Validate and submit promotional materials in compliance with regulations

  • Collaborate with marketing teams to support the development of compliant promotional campaigns

  • Review training modules for medical sales representatives

  • Prepare and follow up on national and European drug registration files

  • Validate and monitor packaging items for regulatory compliance

  • Contribute to drafting therapeutic interest notes for drug market access


Candidate Profile:

  • Experience: Adept at working in fast-paced, collaborative teams

  • Skills:

    • Experience in controlling and validating promotional information

  • Education: Pharmacist Degree with a specialization in Regulatory Affairs

  • Languages: Fluency in both French and English is required