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Medical Device Clinical Research 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 ... clinical research areas Relevant industry certifications preferred (i.e. CCRA, RAC, CDE ...

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 ...

Impulse Dynamics

Clinical Trial Manager

Marlton, NJ

$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 ...

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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 Aug 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 are some of the typical daily responsibilities in a Medical Device Clinical Research role?

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 the Medical Device Clinical Research position, and why are they important?

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.

What is a Medical Device Clinical Research job?

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.

More about Medical Device Clinical Research jobs
What cities are hiring for Medical Device Clinical Research jobs? Cities with the most Medical Device Clinical Research job openings:
What are the most commonly searched types of Medical Device Clinical Research jobs? The most popular types of Medical Device Clinical Research jobs are:
What states have the most Medical Device Clinical Research jobs? States with the most job openings for Medical Device Clinical Research jobs include:
What job categories do people searching Medical Device Clinical Research jobs look for? The top searched job categories for Medical Device Clinical Research jobs are:
Medical Device Clinical Research jobs near you
Infographic showing various Medical Device Clinical Research job openings in the United States as of July 2026, with employment types broken down into 2% As Needed, 73% Full Time, 17% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $107,336 per year, or $51.6 per hour.

Clinical Research Associate (CRA) -Cardiovascular Medical Device

Mirus LLC

Marietta, GA • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 13 days ago

Job description


Role: Clinical Research Associate (CRA) - Cardiovascular Medical Device

Location: Remote

Position Summary:

Assist with the management of cardiovascular clinical studies for MiRus products with a focus on adherence to critical timelines, high-caliber document development and quality data collection. The applicant should possess strong critical thinking skills and the ability to comprehend technical subject matter to effectively contribute to the organization.

Essential Duties and Responsibilities:

  • Contribute to content generation, writing and editing of study protocols, amendments, informed consents, committee charters, study reports, monitoring plans, and other related clinical and regulatory documents.
  • Assist with the management of investigational studies from start through study closure.
  • Engage in new study trial design with cross functional teams, including clinical and pre-clinical research and development groups.
  • Contribute to the development of CRFs
  • Assist with the formulation of instructional materials and training of investigators, study coordinators and associated study site personnel on the conduct of the clinical trials, as applicable.
  • Assist Study Manager with safety monitoring including preparing supporting documentation for CEC and/or DSMB, meetings, agenda, data review, presentations, and updating relevant trackers as applicable.
  • Serve as a point of contact between clinical site investigators and the MiRus team.
  • Work with investigators and site personnel to quickly and effectively resolve discrepancies.
  • May be responsible for patient accruals and tracking payments to sites for clinical study programs
  • Serve as a point of contact between CRO personnel and MiRus.
  • Oversee/support CRO and field study monitors, with monitoring related items and follow-up on study tasks.
  • Monitor ongoing compliance to study protocols in accordance with applicable regulations and GCP, work instructions, guidelines and/or policies.
  • Provide continuous data review of source documents, case report forms, data reports as appropriate.
  • Assist in review of monitoring reports and tracking of action items.
  • Review source documentation to confirm subject eligibility for clinical trials.
  • Track and upload study imaging
  • Manage clinical study documentation (trial master file and study related tracking).
  • Update and design as needed study dashboards, study trackers and other applicable study documents to provide regular updates on trial status to Study Manager
  • Interact with data management, as applicable
  • Support applications and technical files as needed.
  • Assist with preparation for investigators meetings.

Minimum Education and/or Experience:

  • Bachelor’s or Master’s degree in nursing with clinical experience in the cardiac field (CCU, CVOR, Cath Lab) and experience in a clinical research role. CRA certification desired.
  • At least 2 years of experience in clinical research role, with at least 2 years in CRA role, preferably in cardiovascular medical device.
  • Experience in clinical trials and/or post-market registries in the U.S., Australian and/or European Union, with other geographies desired.
  • Current knowledge of medical device clinical trials design and best practices.
  • Proficient knowledge of FDA regulations and ICH/GCP guidelines, guidance documents, and other applicable regulations and standards, and implementation of these standards in the medical device industry, in the U.S. and all countries in which trials are conducted.
  • General application of medical terminology (cardiovascular specific preferred).

Benefits:
MiRus offers competitive compensation, options, full benefits, and relocation assistance.

  • 401(k)
  • Dental insurance
  • Vision insurance
  • Disability insurance
  • Employee assistance program
  • Flexible spending account or Health Savings Account
  • Health insurance
  • Life insurance
  • Paid time off

Schedule:

  • Monday to Friday (8am – 5pm)

Work Location:

  • Remote
  • Position may require domestic travel at least 20-40%