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Clinical Research Associate Cardiac Device Jobs

Provident Research Inc

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Senior Clinical Research Associate Cardiac Medical Device

Los Angeles, CA · Remote

$135K - $141K/yr

SR CRA Cardiac Medical Device (home based) Remote Become Part of a Major Initiative to Monitor Life ... clinical research areas Relevant industry certifications preferred (i.e. CCRA, RAC, CDE ...

Provident Research Inc

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Senior Clinical Research Associate Cardiac Medical Device

Phoenix, AZ · Remote

$135K - $141K/yr

SR CRA Cardiac Medical Device (home based) Remote Become Part of a Major Initiative to Monitor Life ... clinical research areas Relevant industry certifications preferred (i.e. CCRA, RAC, CDE ...

Medasource

$70 - $75/hr

... cardiac, vascular, or neuromodulation technologies. WHAT YOU'LL DO * Monitor clinical studies at ... Ensure timely and accurate reporting of adverse events, protocol deviations, device complaints, and ...

Opis Senior Services Group

Ensuring that device complaints and malfunctions are reported according to Policies and Procedures ... A general familiarity with cardiac, vascular, and/or neuromodulation technologies. * Previous ...

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How much do clinical research associate cardiac device jobs pay per year?

As of Sep 13, 2026, the average yearly pay for clinical research associate cardiac device in the United States is $94,314.00, according to ZipRecruiter salary data. Most workers in this role earn between $62,500.00 and $128,000.00 per year, depending on experience, location, and employer.

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Infographic showing various Clinical Research Associate Cardiac Device job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 71% Full Time, 18% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $94,314 per year, or $45.3 per hour.

Senior Clinical Research Associate Cardiac Medical Device

Los Angeles, CA • Remote

Provident Research Inc
Biotechnology Research and Development • 51 - 200 employees
Learn more about Provident Research Incexternal

$135K - $141K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 27 days ago

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Job description

SR CRA Cardiac Medical Device (home based) Remote

Become Part of a Major Initiative to Monitor Life Saving Cardiovascular Devices

This position will be working with a Provident Research Inc. in a dedicated Functional Source relationship. Interviews are being scheduled now to fill immediate openings. Our client is an Industry Leader in Medical Devices and this role is responsible for managing clinical activities at multiple study sites, as well as fostering strong, productive relationships with colleagues within the Organization.

Previous Medical Device Monitoring is Required.

To qualify, you must have monitored any of the following indications, involving medications or medical devices:

Pacemakers | Anticoagulation Medications | Coronary Stents |Meds for Congestive Heart Failure | Heart Valves AFIB

This position involves a strong understanding of the Heart with the Conditions and Medications that impact patient outcomes. Previous Cardiovascular experience a plus (like stroke, MS, Parkinson's).

Responsible for managing clinical study activities for multiple sites in single or several Clinical Projects. Oversees performance of appointed study sites conducting company initiated clinical studies.

Responsible for the site visits, monitoring, communication and deliverables for the assigned study sites Serves as a member of the clinical study team and is the liaison between Clinical Operations and Study Site personnel for the specific clinical projects.

This opening is immediate due to expansion.

Benefits:

This position affords you an opportunity to experience many different aspects of the clinical development industry. Our client is proud to offer a career pathway that looks to internal candidates for promotion.

For the right individuals, this position offers a competitive salary along with:

  • Medical, Dental, and Vision
  • Disability
  • Life Insurance
  • 401(k) Plan
  • Paid Vacation and Holidays

Education

A Bachelor Degree is required.

Experience

Previous Regional monitoring required

Requires understanding and application of regulations and standards applied in clinical research areas

Relevant industry certifications preferred (i.e. CCRA, RAC, CDE)

Demonstrated competencies in the following areas are required:

  • Leadership
  • Strong Written and Verbal Communications
  • Strong organizational skills
  • Ability to travel Regionally up to 65%
  • Attention to details

Key Job Activities:

  • Build relationships with investigators and site staff
  • Monitor patient safety on-site (review for missing SAEs, AEs, ConMed) and address protocol violations
  • Take responsibility for specific tasks on projects, or acts as the main CRA contact on individual projects
  • Perform on site visits in accordance with the monitoring plan
  • Conduct on-site study-specific training (if applicable)
  • Perform site facilities inspection
  • Monitor and maintain ICH-GCP compliance

Company Description

PRI is dedicated to providing our employees with the tools to succeed. Come and join the movement!