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Medical Device Clinical Research Jobs (NOW HIRING)

Ambu

Clinical Trial Manager

Columbia, MD · On-site

Clinical Research Department: Clinical Affairs Employment Type: Full-time Req ID: 10220 Job Title ... of medical device clinical studies designed to acquire clinical data that supports product ...

Impulse Dynamics

Clinical Trial Manager

Marlton, NJ · On-site

$95K - $115K/yr

Minimum of 2 years of progressive experience in clinical operations, clinical trial management, or project management within the pharmaceutical, biotechnology, medical device, or contract research ...

Iota Biosciences

Manager, Clinical Operations

Alameda, CA · On-site

$145K - $200K/yr

Minimum 8+ years of relevant clinical research experience in the medical device field, or an advanced degree with a minimum of 5 years of relevant experience in the medical device field * At least 3 ...

BiVACOR Inc

Clinical Research Manager

Huntington Beach, CA · On-site

$110K - $150K/yr

As a Clinical Research Manager, you will own end-to-end US IDE study operations, leading a team of ... Class III medical device experience an advantage * Can-do attitude, strategic thinker with strong ...

BiVACOR Inc

Clinical Research Manager

Huntington Beach, CA · On-site

$110K - $150K/yr

As a Clinical Research Manager, you will own end-to-end US IDE study operations, leading a team of ... Class III medical device experience an advantage * Can-do attitude, strategic thinker with strong ...

BiVACOR Inc

Clinical Research Manager

Huntington Beach, CA · On-site

$110 - $150/hr

As Senior Clinical Research Manager, you will own end-to-end US IDE study operations, leading a ... Class III medical device experience an advantage * Can-do attitude, strategic thinker with strong ...

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Medical Device Clinical Research information

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$49K

$107.3K

$189K

How much do medical device clinical research jobs pay per year?

As of Sep 2, 2026, the average yearly pay for medical device clinical research in the United States is $107,336.00, according to ZipRecruiter salary data. Most workers in this role earn between $81,000.00 and $122,500.00 per year, depending on experience, location, and employer.

What is a medical device clinical research?

A Medical Device Clinical Research job involves designing, conducting, and managing clinical studies to evaluate the safety and efficacy of medical devices. Professionals in this role ensure compliance with regulatory guidelines, collect and analyze clinical data, and collaborate with regulatory agencies, investigators, and other stakeholders. Their work supports device approval and post-market surveillance to ensure patient safety.

What are the typical daily responsibilities in medical device clinical research?

In a Medical Device Clinical Research position, your daily tasks often include coordinating and monitoring clinical trials, ensuring compliance with protocols and regulations, and managing study documentation. You may also work closely with investigators, study coordinators, and cross-functional teams to ensure timely data collection and deal with queries related to patient enrollment or safety. Regular interactions with regulatory agencies and contributions to study reports are also common. These responsibilities ensure that clinical trials run smoothly, meet quality standards, and advance the development of medical devices that improve patient care.

What are the key skills and qualifications needed to thrive in medical device clinical research?

To thrive in Medical Device Clinical Research, you need a solid understanding of clinical trial design, regulatory requirements, and data analysis, usually supported by a degree in life sciences or a related field. Familiarity with electronic data capture (EDC) systems, Good Clinical Practice (GCP) certifications, and regulatory submission platforms is typically required. Strong organizational skills, attention to detail, and effective communication set candidates apart in this field. These competencies are crucial to ensure studies are conducted ethically, data is accurate, and regulatory standards are met in developing safe and effective medical devices.

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What are the most commonly searched types of Medical Device Clinical Research jobs?

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Medical Device Clinical Research jobs near you
Infographic showing various Medical Device Clinical Research job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 15% Part Time, and 6% Contract. Highlights an 92% Physical, 1% Hybrid, and 7% Remote job distribution, with an average salary of $107,336 per year, or $51.6 per hour.

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

Re-posted 16 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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