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Local Study Manager – France

3-6 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 Study Manager – France (Full-Time, Permanent)

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

Excelya, a leading European Contract Research Organization (CRO), is seeking a Local Study Manager to oversee clinical trials in oncology for one of the world’s largest pharmaceutical companies. This role involves coordinating local clinical teams, managing study schedules and budgets, ensuring regulatory compliance, and overseeing patient recruitment.

Key Responsibilities

  • Lead the setup, monitoring, and closure of oncology clinical trials.
  • Coordinate the local clinical team and ensure smooth execution of study activities.
  • Prepare clinical study documents and manage regulatory submissions.
  • Oversee the study schedule, budget, and center/subcontractor selection.
  • Ensure patient recruitment targets are met through effective site management.
  • Deliver study results while maintaining quality, compliance, and cost-efficiency.
  • Conduct feasibility studies and investigator selection.
  • Provide operational leadership to a team of Clinical Research Associates.

Minimum Requirements

  • 3 to 6 years of experience in operational and budgetary management of international clinical trials.
  • Experience in oncology or tumor biomarkers.
  • Strong organizational, leadership, and communication skills.
  • Fluent in English with strong scientific expertise.

Location: Paris Area, France

This is an excellent opportunity for an experienced Clinical Study Manager to work on high-impact oncology trials in a dynamic, collaborative environment.