Senior Site Study Coordinator
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Role: Senior Site Study Coordinator (Non-Patient Facing)
Location: Montpellier, France
Language: Fluent in French and English
Work Mode: 100% On-Site
Hiring Type: Freelance / B2B Contract
Duration: 6months (expected for long-term)
Capacity: 8hours per day / 40hours per week
Les candidats doivent prendre le temps de lire attentivement tous les éléments de cette annonce d'emploi. Veuillez postuler rapidement.
Position Overview: The Senior Site Study Coordinator (Non-Patient Facing) provides advanced administrative support and oversight for clinical research studies. This senior role includes managing study operations, supervising junior coordinators, and ensuring high standards of regulatory compliance and study documentation.
Exp: 7-8 years in similar profile
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.
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