Clinical Research Associate

Metric Bio; Massachusetts; On-site; USD 100,000 - 150,000; Full time

Benefits offered by this job

Significant ownership across U.S. CLin

Cross-functional exposure

Growth opportunities

Job summary

Metric Bio is seeking a Senior Clinical Research Associate to lead U.S. cardiovascular device clinical programs. You will own site management from activation through enrollment, working closely with investigators and internal teams to drive studies forward.

The role emphasizes broad involvement across Clinical, Regulatory and R&D, not just monitoring, with opportunities for long-term growth and a competitive compensation package.

Qualifications

• Extensive clinical research and monitoring experience in medical devices.
• Understanding of GCP, FDA and IRB requirements; IDE exposure valued.

Responsibilities

• Manage full spectrum of study execution from site activation to enrollment and data quality.
• Collaborate with investigators, sites and internal teams (Regulatory, R&D) to drive studies forward.
• Ensure regulatory documentation and study submissions meet requirements.
• Travel to clinical sites across the U.S. as needed.

Skills

Clinical research

Independent site monitoring

GCP FDA IRB knowledge

Travel to sites

Job description

I'm hiring a Senior Clinical Research Associate to join a growing cardiovascular medical device company developing innovative technologies designed to improve the treatment of structural heart disease.

This is an opportunity to take meaningful ownership of U.S. clinical studies at a company progressing innovative technology through clinical development and commercialization. Rather than operating as a traditional monitoring-focused CRA, you'll work closely with investigators, clinical sites and internal Clinical, Regulatory and R&D teams to help drive studies forward.

The role will cover the full spectrum of study execution, from site start-up and activation through enrollment, ongoing site management, data quality and regulatory documentation.

This opportunity offers:

• Significant ownership and visibility across U.S. clinical programs
• Broad involvement across Clinical, Regulatory and R&D rather than a narrow monitoring role
• The opportunity to join a growing international MedTech company at an important stage of U.S. expansion
• Long-term growth opportunities
• A competitive compensation package

I'm looking for someone with:

• Strong clinical research and independent site monitoring experience
• Medical device experience, ideally within cardiovascular, Structural Heart or Interventional Cardiology
• Knowledge of GCP, FDA and IRB requirements, with IDE exposure highly valuable
• Experience supporting study documentation, data quality and clinical/regulatory submissions
• The ability to work independently and travel to clinical sites across the U.S.