Sr. Manager, Clinical Site Development

Core Responsibilities:

• Execute clinical site development strategy across assigned sites, assessing investigator experience, patient volume, and research infrastructure.
• Support site activation, enrollment pathways, and resolution of operational barriers.
• Maintain regular communication with sites and provide timely updates to senior management.

Collaboration & Compliance:

• Work with cross-functional teams, CROs, and site staff to coordinate trial execution.
• Ensure all activities follow Good Clinical Practice, IDE requirements, and Company SOPs.
• Conduct site visits and support investigator meetings, grand rounds, and educational programs.

Qualifications & Experience:

• Bachelor's degree preferred with 8+ years in clinical research, site management, or related field.
• Experience in medical device trials, cardiac surgery, electrophysiology, or interventional cardiology preferred.
• Strong understanding of patient recruitment, enrollment, and site development processes.

Compensation & Culture:

• Competitive benefits including health insurance, 401(k), stock options, ESPP, and paid time off.
• Innovative, inclusive culture with growth opportunities and wellness programs.
• Equal opportunity employer committed to diversity and reasonable accommodations.