Senior Site Study Coordinator

Il y a 1 jour

Montpellier, Occitanie, France MPower Plus Temps plein

Role: Senior Site Study Coordinator (Non-Patient Facing)

Location: Montpellier, France(Onsite)

Contract : 12+ Months contract



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Key Responsibilities:

  • Provide advanced administrative support for clinical research studies.
  • Oversee study operations and ensure compliance with protocols and regulatory requirements.
  • Supervise and mentor junior study coordinators.
  • Maintain high standards of study documentation and record-keeping.
  • Collaborate with Principal Investigators (PIs), study teams, and sponsors to ensure study success.
  • Prepare and manage regulatory submissions and communications.
  • Monitor and report on study progress and key performance indicators.

Qualifications:

  • Bachelor's degree in life sciences, healthcare, or related field; advanced degree preferred.
  • Extensive experience in clinical research coordination and administration.
  • Strong leadership and management skills. xuezdbg
  • In-depth knowledge of regulatory requirements and Good Clinical Practice (GCP)
  • Excellent organizational, communication, and problem-solving skills.