Clinical Trial Manager

Metric Bio; Boston (MA); On-site; USD 110,000 - 170,000; Full time

Job summary

Metric Bio in the Boston area is seeking a Clinical Trial Manager to lead U.S. clinical programs for a growing medical device company focused on Structural Heart technology.

This hands-on CTM role emphasizes study execution, site visits, CRO oversight, and collaboration with Clinical, Regulatory, R&D and quality teams to advance IDE and post‑market studies.

You will build investigator relationships, travel to U.S. sites, and take ownership at a pivotal stage of product development.

Qualifications

• 5+ years of clinical research in medical devices.
• Experience leading study execution and managing CROs/CRAs.
• Strong relationships with investigators and sites.
• Willingness to travel frequently within the U.S.

Responsibilities

• Drive study execution and milestones across U.S. clinical programs.
• Oversee CROs, CRAs and other clinical partners.
• Collaborate across Clinical, Regulatory, R&D and Quality teams.

Skills

Clinical research

CTM experience

US IDE studies

Cardiovascular devices

Investigator/site relationships

Travel frequently

Job description

I'm hiring a Clinical Trial Manager to join a well-backed, growing medical device company developing innovative technology within Structural Heart. With expanding U.S. clinical activity and important studies progressing, this is an opportunity to become a key part of the organisation at an important stage of its development.

You'll become a key U.S. Clinical Operations representative, taking meaningful ownership of U.S. clinical programs and working directly with leading investigators and research teams. This is deliberately a hands‑on CTM role: You'll drive study execution and key milestones while maintaining a strong presence at clinical sites and overseeing CROs, CRAs and other clinical partners.

The opportunity offers significantly more visibility and ownership than a traditional monitoring-focused position. You'll work closely across Clinical, Regulatory, R&D, Quality and the U.S. field team, directly contributing to the progression of innovative cardiovascular technology through U.S. IDE and post-market studies.

Key experience:

• 5+ years of clinical research experience specifically within medical devices.
• CTM experience or a strong Senior/Lead CRA ready to take broader ownership of study execution.
• Experience with U.S. IDE studies strongly preferred.
• Cardiovascular device experience, ideally within Structural Heart or Interventional Cardiology.
• Strong investigator/site relationships with experience overseeing CROs, CRAs and/or clinical vendors.
• Highly independent and hands‑on, with the flexibility to travel frequently to U.S. clinical sites.