Senior Site Study Coordinator

Il y a 4 semaines

Montpellier, Occitanie, France MPower Plus Temps plein

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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.