Cardiovascular MedTech Regulatory Strategy VP

IQVIA; Washington (District of Columbia); On-site; USD 169,000 - 472,000; Full time

Job summary

IQVIA MedTech is seeking a Vice President, MedTech Cardiovascular Regulatory Affairs to lead regulatory strategy and submissions for a comprehensive client portfolio. You will mentor teams, manage client relationships, and drive regulatory programs across medical devices and diagnostics while collaborating with multiple IQVIA departments.

Ideal candidates bring fifteen+ years in Regulatory Affairs for medical devices or biologics, strong leadership, and deep FDA/Notified Body knowledge.

Qualifications

• Bachelor’s degree in a scientific, engineering, or regulatory discipline required or equivalent.
• MS or PhD preferred for leadership in regulatory affairs.

Responsibilities

• Develop and lead regulatory submissions and strategy for medical devices and related products.
• Manage department budgets, client relationships, and cross-functional teams.
• Mentor junior staff and lead multiple regulatory projects with external stakeholders.
• Collaborate with clinical, quality assurance, and compliance functions to ensure compliant submissions.

Skills

Regulatory leadership

Regulatory strategy

Regulatory submissions

Client relationships

Mentoring

Education

Bachelor's degree in a scientific, engineering, or regulatory discipline

MS or PhD preferred

Tools

MS Office

Excel

Word

PowerPoint

Job description

IQVIA MedTech is seeking a Vice President, MedTech Cardiovascular Regulatory Affairs to lead regulatory strategy and submissions for a comprehensive client portfolio. You will mentor teams, manage client relationships, and drive regulatory programs across medical devices and diagnostics while collaborating with multiple IQVIA departments.

Ideal candidates bring fifteen+ years in Regulatory Affairs for medical devices or biologics, strong leadership, and deep FDA/Notified Body knowledge.