Lead Trial Manager: Oncology/Cardio/Endo/Metabolic

Medpace, Inc.; Lyon; Hybride; EUR 70 000 - 110 000; Plein temps

Avantages offerts par ce poste

Competitive compensation

Equity grants

Remote work potential

Résumé du poste

Medpace is seeking a Clinical Trial Manager in Lyon to lead trials across Oncology, Cardiovascular, Endocrine and Metabolic areas. The role includes potential remote work for eligible experience and requires strong leadership in a fast-paced CRO environment.

You will manage day-to-day operations, ensure ICH/GCP compliance, and act as the Sponsor contact for study deliverables, timelines, and vendors. Fluency in French and English is required.

Qualifications

• Bachelor’s degree in a health or life sciences field; advanced degree preferred.
• 5+ years of Clinical Trial Management experience, CRO experience preferred.
• Experience in Phases 1-4; Phases 2-3 preferred.
• Ability to manage overall project timelines and bid defenses is a plus.
• Fluent in French and English.

Responsabilités

• Manage day-to-day project operations per contract and ICH/GCP standards.
• Serve as primary Sponsor contact for operational issues and study deliverables.
• Maintain knowledge of protocol, therapeutic area, and indication.
• Provide cross-functional oversight of internal project team and training.
• Review study protocol, edit check specifications, data analysis plan, and reports.
• Develop operational project plans.
• Manage risk assessment and execution.
• Manage study vendors.
• Oversee site quality and supervise CRAs and monitoring deliverables.

Connaissances

Fluent French

Fluent English

Leadership

Formation

Bachelor’s degree in health/life sciences

Advanced degree preferred

Description du poste

Medpace is seeking a Clinical Trial Manager in Lyon to lead trials across Oncology, Cardiovascular, Endocrine and Metabolic areas. The role includes potential remote work for eligible experience and requires strong leadership in a fast-paced CRO environment.

You will manage day-to-day operations, ensure ICH/GCP compliance, and act as the Sponsor contact for study deliverables, timelines, and vendors. Fluency in French and English is required.