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Medical Device Cra Jobs (NOW HIRING)

Provident Research Inc

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Senior Clinical Research Associate Cardiac Medical Device

New York, NY · 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

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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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All JobsMedical Device Cra Jobs

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
Clinical Research Associate (Physical Therapist Candidates)

Clinical Research Associate (Physical Therapist Candidates)

Medpace, Inc.

Cincinnati, OH • On-site

Other

Medical, Retirement, PTO

Posted 25 days ago

Medpace rating

8.4

Company rating: 8.4 out of 10

Based on 8 frontline employees who took The Breakroom Quiz

15th of 57 rated research

Job description

Job Summary
We are hiring Physical Therapists at Medpace!
The Clinical Research Associate position at Medpace offers the unique opportunity to have an exciting career in the research of drug and medical device development while making a difference in the lives of those around them. For those with a physical therapy/kinesiology background who want to explore the research field, travel the US, and be part of a team bringing pharmaceutical and medical devices to market - this could be the right opportunity for you!
Positions are office based in Cincinnati-OH, Dallas-TX, or Denver-CO.
MEDPACE CRA TRAINING PROGRAM (PACE®)
No research experience is needed as Medpace provides comprehensive initial and ongoing training, unmatched by other CROs. Through our PACE® Training Program, you will join other Professionals Achieving CRA Excellence:
  • PACE® provides the platform to effectively and confidently carry out your duties, enhance your current abilities and ultimately help you become a high-functioning independent Medpace CRA
  • PACE® will prepare you by developing your CRA skills through interactive discussions and hands on job-related exercises and practicums.
  • To supplement your in-house and field-based training you may also participate in other clinical research departmental core rotations, learning other aspects of the drug/device development and approval process.

WHY BECOME A CRA
This role takes you on a journey through travel and excitement which will allow you to make a difference on a large scale through the enhancement of pharmaceuticals and medical devices. The CRA position provides many other distinctive advantages including:
  • Dynamic working environment, with varying responsibilities day-to-day
  • Expansive experience in multiple therapeutic areas
  • Work within a team of therapeutic and regulatory experts
  • Defined CRA promotion and growth ladder with potential for mentoring and management advancements
  • Competitive pay and many additional perks unmached by other CROs (SEE BELOW)

WE OFFER THE FOLLOWING
  • Competitive travel bonus;
  • Equity/Stock Option program;
  • Training completion and retention bonus
  • Annual merit increases;
  • 401K matching;
  • The opportunity to work from home;
  • Flexible work hours across days within a week;
  • Retain airline reward miles and hotel reward points;
  • Home office furniture allowance, laptop, mobile phone with hotspot for internet access anywhere;
  • In-house travel agents, reimbursement for airline club, and TSA pre-check,
  • Opportunity for leadership positions - Lead CRA, CRA Manager, Training and Development Manager, and many more;
  • CRA Training program;
  • Ongoing therapeutic training by our in-house physicians who are medical and regulatory experts;
  • In-house administrative support for all levels of CRAs; and
  • Opportunities to work with international team of CRAs.

Responsibilities
  • Conduct qualification, initiation, monitoring, and closeout visits at research sites in compliance with the approved protocol;
  • Communication with the medical site staff including coordinators, clinical research physicians, and their site staff;
  • Verify adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff;
  • Medical record and research source documentation verification against case report form data, including informing the site staff of any entry errors, ensuring good documentation practices are being adhered to and communicating protocol deviations appropriately per SOPs, GCP, and applicable regulatory requirements;
  • Verification that the investigator is enrolling only eligible subjects;
  • Regulatory document review;
  • Medical device and/or investigational product/drug accountability and inventory;
  • Verification and review of adverse events, serious adverse events, concomitant medications and corresponding illnesses to confirm accurate data reporting in accordance with the protocol;
  • Assess the clinical research site's patient recruitment and retention success and offering suggestions for improvement; and
  • Completion of monitoring reports and follow-up letters, which includes providing summaries of the significant findings, deviations, deficiencies, and recommended actions to secure compliance.

Qualifications
  • Must have a minimum of a Bachelor's degree in a health or science related field; degree in Physical Therapy or Kinesiology preferred;
  • Ability to travel 60-70% to locations nationwide is required;
  • Must maintain a valid driver's license and the ability to drive to monitoring sites;
  • Minimum 1 year healthcare-related work experience preferred;
  • Proficient knowledge of Microsoft® Office;
  • Strong communication and presentation skills; and
  • Must be detail-oriented and efficient in time management.

Medpace Overview
Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 6,000 people across 40+ countries.
Why Medpace?
People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.
The work we've done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.
Cincinnati Perks
  • Cincinnati Campus Overview
  • Flexible work environment
  • Competitive PTO packages, starting at 20+ days
  • Competitive compensation and benefits package
  • Company-sponsored employee appreciation events
  • Employee health and wellness initiatives
  • Community involvement with local nonprofit organizations
  • Discounts on local sports games, fitness gyms and attractions
  • Modern, ecofriendly campus with an on-site fitness center
  • Structured career paths with opportunities for professional growth
  • Discounted tuition for UC online programs

Awards
  • Named a Top Workplace in 2024 by The Cincinnati Enquirer
  • Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024
  • Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility

What to Expect Next
A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.
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About Medpace

Sourced by ZipRecruiter

Medpace is a globally recognized clinicial contract research organization (CRO) based in Cincinnati, OH, in the United States. Established in 1992, it operates in the healthcare sector, providing scientifically-driven outsourcing solutions for the development of drugs and medical devices. It offers comprehensive services like full-service clinical development services, regulatory affairs management, clinical pharmacology, data management, statistical analysis, and medical writing. By applying a scientifically-driven, therapeutically-focused, and patient-centric approach, Medpace's mission is to accelerate the global development of safe and effective medical therapies.

Industry

Medical equipment and supplies manufacturing

Company size

1,001 - 5,000 Employees

Headquarters location

Cincinnati, OH, US

Year founded

1992

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