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Local Clinical Trial Assistant – France

2+ 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

Local Clinical Trial Assistant – France (Full-Time, Permanent)

Excelya | Full-Time | Permanent | Paris Area, France

Excelya, a leading European Contract Research Organization (CRO), is looking for a Local Clinical Trial Assistant to provide administrative, budgetary, and documentation support for clinical trials. This role involves collaborating closely with Project Managers and Clinical Research Associates to ensure the smooth execution of clinical studies.

Key Responsibilities

  • Administrative and financial support throughout all clinical trial phases (set-up, follow-up, and closure).
  • Participate in project team meetings and assist in coordination efforts.
  • Manage eTMF documentation (Veeva Vault):
    • Upload clinical trial documents.
    • Perform quality control to ensure compliance.

Minimum Requirements

  • At least 2 years of experience as a Clinical Trial Assistant in a pharmaceutical company.
  • Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint).
  • Experience with eTMF systems (Veeva Vault or similar).
  • Ability to quickly adapt to system tools such as SAP/iBuy, CTMS Veeva Vault, DocuSign.
  • Strong teamwork, adaptability, and multitasking skills.
  • Attention to detail with a focus on quality control.

Location: Paris Area, France

This position is ideal for an organized and detail-oriented professional looking to grow within the clinical research industry.