ZipRecruiter

Log In

2

Remote Medical Device Clinical Research Jobs (NOW HIRING)

Provident Research Inc

Be Seen First

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 ...

ICON

Study Start Up Associate - Medical Device

Blue Bell, PA · On-site +1

$32 - $43.75/hr

Study Start Up Associate - Medical Device - Home Based (US) ICON is a global healthcare ... Must be comfortable interacting with clinical research site personnel via phone and email. * Remote ...

next page

Showing results 1-20

All JobsMedical Device Clinical Research JobsRemote Medical Device Clinical Research Jobs

Remote Medical Device Clinical Research information

See salary details

$49K

$107.3K

$189K

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

As of Jul 30, 2026, the average yearly pay for remote 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 the difference between Remote Medical Device Clinical Research vs Remote Medical Device Regulatory Affairs Specialist?

AspectRemote Medical Device Clinical ResearchRemote Medical Device Regulatory Affairs Specialist
Required CredentialsClinical research certifications, life sciences degreeRegulatory affairs certifications, life sciences or legal background
Work EnvironmentClinical trial sites, remote data managementRegulatory agencies, company offices, remote documentation
Employer & Industry UsageMedical device companies, CROs, hospitalsMedical device manufacturers, regulatory bodies
Common Search & ComparisonYesYes

Remote Medical Device Clinical Research involves managing and conducting clinical trials to test medical devices, focusing on patient safety and data collection. In contrast, Remote Medical Device Regulatory Affairs Specialists handle compliance, documentation, and submissions to regulatory agencies. Both roles require specialized certifications and are integral to bringing medical devices to market, but they focus on different stages of the product lifecycle.

More about Remote Medical Device Clinical Research jobs
What cities are hiring for Remote Medical Device Clinical Research jobs? Cities with the most Remote 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 Remote Medical Device Clinical Research jobs? States with the most job openings for Remote Medical Device Clinical Research jobs include:
What job categories do people searching Remote Medical Device Clinical Research jobs look for? The top searched job categories for Remote Medical Device Clinical Research jobs are:
Remote Medical Device Clinical Research jobs near you
Infographic showing various Remote 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.

Senior Clinical Research Associate Cardiac Medical Device

Provident Research Inc

Phoenix, AZ • Remote

$135K - $141K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 4 days ago

Be Seen First

After you apply to this job, you can share why you’re interested to jump to the top of the candidate list.

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

PRI is dedicated to providing our employees with the tools to succeed. Come and join the movement!