PMCF Strategy Lead — Medical Device Evidence & Reporting

Intuitive; Sunnyvale (CA); On-site; USD 97,600 - 140,400; Full time

Job summary

A global medical device company is seeking a Post Market Clinical Follow up Specialist to lead and execute PMCF strategies. The successful candidate will manage cross-functional teams, ensuring compliance with regulatory requirements. This role requires a strong background in clinical research and the ability to develop innovative evidence strategies. Candidates should have an undergraduate degree in engineering or life sciences and extensive experience. The position is based in Sunnyvale, CA with a competitive salary range of $97,600 to $140,400.

Qualifications

• 4+ years of related experience preferred.
• Knowledge of EU Medical Device Regulation (MDR) is essential.
• Experience in medical device clinical research and data analysis.

Responsibilities

• Lead development of PMCF strategies with teams.
• Create and maintain PMCF Plans.
• Monitor PMCF activities to ensure compliance.

Skills

Project Management

Clinical Research

Technical Writing

Statistical Analysis

Communication

Education

Undergraduate degree in engineering or life science

Tools

Microsoft Excel

Microsoft Word

PowerPoint

Job description

A global medical device company is seeking a Post Market Clinical Follow up Specialist to lead and execute PMCF strategies. The successful candidate will manage cross-functional teams, ensuring compliance with regulatory requirements. This role requires a strong background in clinical research and the ability to develop innovative evidence strategies. Candidates should have an undergraduate degree in engineering or life sciences and extensive experience. The position is based in Sunnyvale, CA with a competitive salary range of $97,600 to $140,400.