Global Clinical Operations Leader — International MedTech

Echosens; Paris; On-site; EUR 110,000 - 140,000; Full time

Job summary

Echosens in Paris is seeking a Global Clinical Operations Manager to lead an international clinical operations team and drive high‑quality worldwide studies. You will oversee sponsor‑driven and IIS programs, ensure compliance with ICH‑GCP, ISO 14155, MDR, and FDA requirements, and shape the clinical evidence strategy in collaboration with Medical Affairs and R&D.

You will mentor teams across regions, manage budgets and timelines, and foster cross‑functional partnerships with investigators,

Qualifications

• MD, PharmD, PhD, or MSc in Life Sciences (or related) with extensive international clinical research experience.
• Experience leading international multicenter clinical studies (sponsor-driven and IIS).
• Strong understanding of international clinical research regulations and evidence generation.

Responsibilities

• Lead Global Clinical Operations and define the strategic operational plan for studies worldwide.
• Manage an international Clinical Operations team and drive collaboration across functions.
• Build Investigator‑Initiated Studies programs and develop long-term investigator partnerships.
• Contribute to clinical strategy with Medical Affairs, R&D, Regulatory Affairs, and investigators.
• Collaborate across R&D, Quality, Medical Affairs, and other departments to support evidence generation.

Skills

Leadership

People management

Clinical operations

International collaboration

Regulatory knowledge

Education

MD/PhD/PharmD/Life Sciences MSc

Job description

Echosens in Paris is seeking a Global Clinical Operations Manager to lead an international clinical operations team and drive high‑quality worldwide studies. You will oversee sponsor‑driven and IIS programs, ensure compliance with ICH‑GCP, ISO 14155, MDR, and FDA requirements, and shape the clinical evidence strategy in collaboration with Medical Affairs and R&D.

You will mentor teams across regions, manage budgets and timelines, and foster cross‑functional partnerships with investigators,