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Clinical Study Support Officer – 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

Clinical Study Support Officer – France
Slug: clinical-study-support-officer-france-excelya

Position: Clinical Study Support Officer
Type: Full-time, Permanent
Location: France
Company: Excelya


Why Join Excelya:
Excelya is a young and dynamic healthcare company with over 900 professionals ("Excelyates") committed to becoming Europe’s leading mid-size CRO. The company stands out through its one-stop service model, which includes full-service solutions, functional service provision, and expert consulting. At Excelya, employees grow alongside top-tier experts, continuously pushing the boundaries of science and healthcare.


About the Role:
The Clinical Study Support Officer plays a vital operational role within the Clinical Supplies Trial Management team. This position involves supporting multiple clinical studies (Phases I–IV) and contributing to key follow-up activities with minimal supervision. It is an opportunity to be a part of a high-energy, collaborative environment that values bold thinking, personal growth, and impactful work in clinical research.


Key Responsibilities:

  • Provide operational support to Clinical Supplies Study Managers (CSSMs) and Clinical Study Supply Leads (CSSLs) across multiple trials

  • Manage clinical supply processes including stock tracking, shipments, returns, and destruction

  • Maintain tracking tools, dashboards, and study-related documentation

  • Coordinate with internal departments (clinical, quality, regulatory) and external partners (CROs, CMOs)

  • Prepare and submit regular status updates and reports

  • Identify and assist in resolving supply-related or operational issues

  • Ensure compliance with company SOPs and clinical supply management processes


Candidate Profile:

  • Experience: Ability to thrive in collaborative, fast-paced settings

  • Skills:

    • Basic knowledge of GxP and GMP

    • Proficient in Microsoft Office, particularly Excel and SharePoint

  • Education: Degree in Life Sciences, Pharmacy, Supply Chain, or a related field (from technical diploma to Master’s level)

  • Languages: Professional fluency in English is mandatory