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Medical Device Cra Jobs (NOW HIRING)

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

Provident Research Inc

Be Seen First

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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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 29, 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.

More about Medical Device Cra jobs
What cities are hiring for Medical Device Cra jobs? Cities with the most Medical Device Cra job openings:
What states have the most Medical Device Cra jobs? States with the most job openings for Medical Device Cra jobs include:
What job categories do people searching Medical Device Cra jobs look for? The top searched job categories for Medical Device Cra jobs are:
Medical Device Cra jobs near you
Infographic showing various Medical Device Cra job openings in the United States as of June 2026, with employment types broken down into 84% Full Time, 3% Part Time, 3% Temporary, and 10% Contract. Highlights an 85% Physical, 3% Hybrid, and 12% Remote job distribution, with an average salary of $79,437 per year, or $38.2 per hour.
Principal Clinical Research Associate (Remote)

Principal Clinical Research Associate (Remote)

Astrix Inc

Cleveland, OH • On-site, Remote

$65 - $80/hr

Full-time

Posted 18 days ago

Key responsibilities

  • Conduct comprehensive monitoring visits (PSV, SIV, RM, COV) across the country.

  • Manage a high volume of site activities, ensuring adherence to protocols, IDE regulations, and ISO 14155 standards.

  • Drive enrollment and oversee long-term patient follow-up for complex device studies.

Job description

Pay Rate Low: 75 | Pay Rate High: 85
We are seeking a high-level, technically proficient Principal CRA to oversee complex monitoring activities for specialized Medical Device trials.
Job Title: Senior / Principal Clinical Research Associate (Medical Device)
Term: 12-Month Renewable Contract (Plus Benefits)
Compensation: $65-80/hr
Travel: Approximately 60% The Role
We are seeking a high-level, technically proficient Senior or Principal CRA to oversee complex monitoring activities for specialized Medical Device trials. Unlike high-volume CRO environments, this role requires a "hands-on" expert who possesses the deep clinical intuition and technical skills that only come with years of dedicated field experience.
You will manage site performance across the country, focusing on high-enrollment sites and long-term follow-up monitoring.
What Sets You Apart
  • True Seniority: You have 5+ years of experience and have mastered the nuances of site management. You are looking for a role where your actual skill set-not just your title-is utilized.
  • Medical Device Expertise: You have a proven track record specifically in the Medical Device sector. Experience in Cardiology is a significant advantage.
  • Site Management Prowess: You prioritize site health and data integrity over "checking boxes." You excel at managing site volume, patient enrollment, and rigorous long-term monitoring.
  • Stability: Your career history reflects commitment and steady growth rather than rapid-fire jumping or title inflation.
Core Responsibilities
  • Conduct comprehensive monitoring visits (PSV, SIV, RM, COV) across country
  • Manage a high volume of site activities, ensuring adherence to protocols, IDE regulations, and ISO 14155 standards.
  • Drive enrollment and oversee long-term patient follow-up for complex device studies.
  • Act as a primary liaison for clinical sites, fostering strong investigator relationships.
Qualifications
  • Minimum 5+ years of CRA experience (must be at a Senior or Principal level).
  • Direct Medical Device monitoring experience is required.
  • Cardiology therapeutic experience is highly preferred.
  • Experience outside of "Big CRO" environments is preferred; we value versatile talent capable of working independently.
  • Ability to travel 60% of the time (approx. 2 weeks/month).
  • Must be based in the U.S.; Central Time Zone is a plus to bridge Eastern and Western engagements.
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