Clinical Operations Lead — Study Delivery & Compliance

Excelya; Paris; Sur place; EUR 60 000 - 80 000; Plein temps

Résumé du poste

A clinical research organization is seeking a professional to lead and coordinate clinical studies in Paris. The ideal candidate has a minimum of 5 years of experience in clinical monitoring and study management, with strong leadership and communication skills. This role involves acting as the liaison between project teams and clinical sites, overseeing monitoring visits, and mentoring Clinical Research Associates. A Bachelor’s degree in life sciences or medicine is required, along with bilingual proficiency in French and English.

Prestations

Innovation-driven work environment

Diverse project opportunities

Focus on personal growth and development

Qualifications

• Minimum of 5 years of experience in clinical monitoring and study management.
• Prior experience as a CRA or in a lead role is highly desirable.
• Bilingual in French and proficient in English.

Responsabilités

• Lead and coordinate the operational aspects of assigned clinical studies.
• Act as the primary liaison between project teams and clinical sites.
• Oversee the planning and execution of monitoring visits.
• Train and mentor Clinical Research Associates.
• Review study-related documents for regulatory compliance.
• Support the management of study budgets and timelines.
• Ensure site staff are knowledgeable about study protocols.
• Facilitate problem-solving and risk assessment during the study.

Connaissances

Strong understanding of GCP

Leadership skills

Excellent communication

Interpersonal skills

Proficiency in CTMS and EDC systems

Formation

Bachelor’s degree in life sciences or medicine

Description du poste

A clinical research organization is seeking a professional to lead and coordinate clinical studies in Paris. The ideal candidate has a minimum of 5 years of experience in clinical monitoring and study management, with strong leadership and communication skills. This role involves acting as the liaison between project teams and clinical sites, overseeing monitoring visits, and mentoring Clinical Research Associates. A Bachelor’s degree in life sciences or medicine is required, along with bilingual proficiency in French and English.