Senior Site Study Coordinator

CosMicIT; Montpellier; Sur place; EUR 55 000 - 70 000; Plein temps

Résumé du poste

CosMicIT is seeking a Senior Site Study Coordinator (Non-Patient Facing) to provide advanced administrative support and oversight for clinical research studies at our Montpellier site. You will manage study operations, oversee junior coordinators, and ensure regulatory compliance and meticulous study documentation.

Ideal candidates will have 7+ years in clinical research coordination, a life sciences or related degree, and strong leadership with a solid grasp of GCP.

Qualifications

• 7+ years of clinical research coordination experience.
• Bachelor's degree; advanced degree preferred.
• Strong leadership and management skills.
• In-depth knowledge of regulatory requirements and GCP.
• Excellent organizational, communication, and problem-solving skills.

Responsabilités

• 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.

Connaissances

Leadership

Regulatory knowledge (GCP)

Organizational skills

Communication skills

Problem-solving

Formation

Bachelor's degree in life sciences, healthcare, or related field

Description du poste

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.

About the Role

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.

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.
• In-depth knowledge of regulatory requirements and Good Clinical Practice (GCP).
• Excellent organizational, communication, and problem-solving skills.
• Experience: 7+ years.

Required Skills

• Strong leadership and management skills.
• In-depth knowledge of regulatory requirements and Good Clinical Practice (GCP).
• Excellent organizational, communication, and problem-solving skills.

Preferred Skills

• Language Preference: Primarily English, with French as the local language.

Pay range and compensation package

[Pay range or salary or compensation]

Equal Opportunity Statement

[Include a statement on commitment to diversity and inclusivity.]