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Senior Clinical Research Associate

United States

Job Title: Senior Clinical Research Associate (Sr. CRA)
Location: Remote (Eastern or Central Time Zone, U.S.)
Travel: ~50%

 

About the Role

We are seeking an experienced Senior Clinical Research Associate (Sr. CRA) to support clinical trials for an innovative cardiovascular medical device portfolio. This individual will play a critical role in ensuring the successful execution of clinical studies, maintaining compliance with regulatory requirements, and driving high-quality data collection across investigative sites.

 

Key Responsibilities

  • Independently manage all aspects of site monitoring activities, including site qualification, initiation, routine monitoring, and close-out visits
  • Oversee approximately 10 clinical trial sites, ensuring adherence to study protocols, GCP, and applicable regulatory requirements
  • Build and maintain strong relationships with investigators and site staff to support enrollment, retention, and overall study success
  • Perform source data verification (SDV) and ensure data integrity, accuracy, and completeness
  • Identify, document, and resolve protocol deviations, data queries, and site performance issues
  • Provide site training and ongoing support for study-related procedures and compliance expectations
  • Collaborate cross-functionally with Clinical Operations, Data Management, Regulatory, and Medical Affairs teams
  • Assist with site management responsibilities, including tracking site performance metrics and supporting risk mitigation strategies
  • Contribute to study documentation, including monitoring reports, trip reports, and audit readiness activities

 

Qualifications

  • Bachelor’s degree in life sciences, nursing, or related field
  • 4+ years of clinical monitoring experience, with at least 1–2 years in a senior-level or lead CRA capacity
  • Experience in cardiovascular studies and/or medical device trials strongly preferred
  • Strong knowledge of ICH-GCP guidelines, FDA regulations, and clinical trial processes
  • Proven ability to manage multiple sites and prioritize workload effectively
  • Excellent communication, organizational, and problem-solving skills
  • Ability to travel up to 50% as required

 

Preferred Qualifications

  • Experience with complex interventional cardiovascular device trials (e.g., structural heart, electrophysiology, or vascular interventions)
  • Prior involvement in site management or mentoring junior CRAs
  • Experience working in a fast-paced, growth-stage company environment

 

What We Offer

  • Competitive salary and performance-based incentives
  • Comprehensive benefits package (medical, dental, vision, 401k, etc.)
  • Opportunity to work on cutting-edge cardiovascular technologies that improve patient outcomes
  • Collaborative, mission-driven culture with strong growth potential

 

Equal Opportunity Employer

We are committed to building a diverse and inclusive workplace and welcome applicants from all backgrounds.

 

If you’re a driven CRA looking to take the next step in your career and make a meaningful impact in cardiovascular innovation, we encourage you to apply.

Apply Now

Discipline

Device and Diagnostics

Job Ref

PR/030179

Published

23 days ago

Expiry

26 Apr 2026 23:59

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