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Clinical Research Associate Oncology – 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 Research Associate – Oncology (France, Full-Time, Permanent)

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

Excelya, a leading European Contract Research Organization (CRO), is seeking a Clinical Research Associate (CRA) specializing in Oncology. This role involves conducting and monitoring international interventional studies in the oncology field, ensuring compliance with Good Clinical Practice (GCP) and ICH regulations.

Key Responsibilities

  • Select and set up investigation centers for clinical studies.
  • Monitor clinical trials, including on-site and remote visits.
  • Manage clinical study budgets.
  • Assist with administrative tasks related to clinical trial setup and monitoring.
  • Maintain communication with investigating physicians.
  • Review clinical instructions as required.
  • Prepare investigation centers for audits and inspections.
  • Ensure deviation traceability and compliance with regulations.

Minimum Requirements

  • Scientific degree (Bac +5 or higher) with Clinical Research Associate (CRA) training.
  • At least 2 years of experience as a CRA monitor in oncology.
  • Strong knowledge of Good Clinical Practice (GCP) and ICH regulations.
  • Autonomous, team-oriented, with strong interpersonal skills.

Location: Paris Area, France

This position is ideal for a dedicated CRA with oncology experience looking to contribute to cutting-edge international clinical studies.