Clinical Study Lead - Regulatory Trials & Protocols

Intuitive Surgical; United States; Remote; USD 120,000 - 180,000; Full time

Job summary

Intuitive Surgical is seeking a senior clinical studies professional to lead evidence generation for regulatory approvals, collaborating with stakeholders and key opinion leaders to design trial protocols and manage execution.

You will oversee site selection, monitoring and data accuracy, ensuring high-quality results. The role includes mentoring junior study managers and driving study meetings and progress toward timely outcomes.

Qualifications

• Advanced degree with 5+ years of clinical research experience.
• Strong knowledge of ICH/GCP and medical device trials.

Responsibilities

• Lead clinical evidence generation and execute clinical studies for regulatory approvals.
• Partner with stakeholders and KOLs to design protocols and manage trial execution.
• Oversee site selection, monitoring, compliance, and data accuracy to ensure high quality.
• Mentor junior study managers and drive study meetings and progress.

Skills

Clinical research

Education

Advanced degree

Job description

Intuitive Surgical is seeking a senior clinical studies professional to lead evidence generation for regulatory approvals, collaborating with stakeholders and key opinion leaders to design trial protocols and manage execution.

You will oversee site selection, monitoring and data accuracy, ensuring high-quality results. The role includes mentoring junior study managers and driving study meetings and progress toward timely outcomes.