Senior Site Study Coordinator
Il y a 1 jour
Montpellier, Occitanie, France
MPower Plus
Temps plein
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Gratuit avec email ou Google
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.