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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 Saving Cardiovascular Devices This position will be working with a Provident Research Inc. in a ...

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OR · On-site

Job Overview: The Senior CRA II is responsible for site monitoring and site management ... nursing certification, medical or laboratory technology. * Thorough knowledge of regulatory ...

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Medical Device Cra information

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$11K

$79.4K

$137.5K

How much do medical device cra jobs pay per year?

As of Jun 9, 2026, the average yearly pay for medical device cra in the United States is $79,437.00, according to ZipRecruiter salary data. Most workers in this role earn between $33,000.00 and $136,500.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Medical Device Clinical Research Associate (CRA), and why are they important?

To thrive as a Medical Device CRA, you need a solid background in life sciences or healthcare, knowledge of clinical trial processes, and typically a bachelor's degree in a related field. Familiarity with electronic data capture (EDC) systems, regulatory guidelines (such as GCP and ISO 14155), and sometimes certifications like ACRP or SOCRA are highly valued. Strong attention to detail, effective communication, and organizational skills help CRAs manage site relationships and ensure compliance. These skills are crucial for maintaining study integrity, meeting regulatory requirements, and safeguarding patient safety throughout clinical trials.

What are some common challenges faced by Medical Device Clinical Research Associates (CRAs) during clinical trials?

Medical Device CRAs often encounter challenges such as ensuring protocol compliance across multiple clinical sites, managing complex documentation requirements, and adapting to frequent regulatory updates. They must also facilitate effective communication between sponsors, investigators, and site staff to maintain trial integrity. Balancing frequent travel with timely data monitoring and issue resolution is another typical aspect of the role, requiring strong organizational and interpersonal skills.

What are Medical Device CRAs?

Medical Device Clinical Research Associates (CRAs) are professionals who oversee and monitor clinical trials involving medical devices to ensure compliance with regulatory requirements and study protocols. They work closely with clinical sites, investigators, and sponsors to verify data accuracy, patient safety, and the proper conduct of the trial. CRAs play a critical role in ensuring that the medical device under investigation is tested ethically and effectively before it reaches the market.

What is the difference between Medical Device Cra vs Clinical Research Associate?

AspectMedical Device CraClinical Research Associate
CertificationsRegulatory knowledge, industry-specific certificationsGCP, ICH certifications, clinical trial training
Work EnvironmentMedical device companies, regulatory agenciesPharmaceutical companies, clinical trial sites
Industry UsageMedical device development and testingDrug and pharmaceutical trials
Common Search/ComparisonRegulatory compliance, device testingTrial monitoring, patient safety

Both roles involve overseeing clinical trials, but Medical Device Cras focus on medical device testing and regulatory compliance, while Clinical Research Associates primarily monitor drug trials and ensure adherence to protocols. Understanding these differences helps professionals choose the right career path or job search focus within clinical research.

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Medical Device Cra jobs near you
Senior Clinical Research Associate Cardiac Medical Device

Senior Clinical Research Associate Cardiac Medical Device

Provident Research Inc

Los Angeles, CA • Remote

$135K - $141K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 20 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

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