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Clinical Study Supply Manager – France

5+ years
Not Disclosed
10 Feb. 10, 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 Supply Manager – France (Full-Time, Permanent Contract)

Excelya | Full-Time | Permanent | France

Excelya, a people-centered CRO founded in 2014, is dedicated to advancing clinical research with care. With a team of 800+ Excelyates, we are on the path to becoming Europe’s leading clinical research organization. Our unique one-stop provider model offers full-service, functional service provider (FSP), and consulting solutions, enabling our team members to thrive in a dynamic and collaborative environment.

We believe in fostering intellectual growth, personal development, and professional excellence, empowering every team member to make a meaningful impact in clinical research.

Position Overview

As a Clinical Study Supply Manager (CSSM), you will play a critical role in the clinical operations department of a major laboratory in Montpellier or Lyon. Your primary responsibility will be the operational management of clinical trial supplies, ensuring timely and compliant delivery while adhering to budgetary constraints and industry regulations.

Key Responsibilities

  • Manage clinical trial supplies to ensure timely and budget-compliant delivery.
  • Ensure compliance with GxP regulations, SOPs, and industry standards.
  • Develop and execute clinical supply strategies for assigned studies.
  • Communicate with study teams to align on clinical supply needs and timelines.
  • Oversee clinical supply production plans and ensure progress according to deadlines.
  • Optimize clinical supply chains and develop risk mitigation strategies.
  • Act as the primary contact for the Global Study Manager, providing leadership and expertise in supply management.
  • Review and contribute to study documentation (e.g., Protocols, Monitoring Plans, Pharmacy Manuals).

Required Skills & Qualifications

  • Experience in clinical operations, preferably on a global scale.
  • Strong organizational and communication skills.
  • Fluent in English to manage global study requirements.
  • Availability to be based in Montpellier, Lyon, or Paris.
  • Immediate availability preferred.

Join Excelya and be part of a team that advances scientific and clinical research while ensuring excellence in clinical supply management!