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Remote Medical Device Clinical Research Jobs (NOW HIRING)

ClinChoice

Senior Clinical Research Associate

... medical device and consumer health companies. We are currently seeking an experienced Senior ... This is a permanent, fully remote position. Candidates must be willing and able to travel to ...

ClinChoice

Senior Clinical Research Associate

... medical device and consumer health companies. We are currently seeking an experienced Senior ... This is a permanent, fully remote position. Candidates must be willing and able to travel to ...

Avania

Clinical Research Associate II x 5

$90K - $110K/yr

Avania is hiring Clinical Research Associates II (CRA II) - Medical Device Clinical Trials Salary ... Ask us about our hybrid and fully remote work opportunities We look forward to receiving your ...

Edwards Lifesciences Corporation

$134K - $190K/yr

Represent the Clinical Affairs Research Team during clinical trial cases with investigating ... Moderate understanding of medical device regulatory requirements and documents, device ...

Edwards Lifesciences Corporation

$134K - $190K/yr

Represent the Clinical Affairs Research Team during clinical trial cases with investigating ... Moderate understanding of medical device regulatory requirements and documents, device ...

IQVIA

Clinical Research Coordinator

Raleigh, NC · Remote

$35 - $42/hr

We partner with the world's leading pharmaceutical, biotechnology, and medical device organizations ... This position is not eligible for employment sponsorship. #LI-CES and #LI-DNP #LI-HCP #remote IQVIA ...

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Remote Medical Device Clinical Research information

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$49K

$107.3K

$189K

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

As of Aug 21, 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.

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The most popular types of Medical Device Clinical Research jobs are:

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Remote Medical Device Clinical Research jobs near you
Infographic showing various Remote Medical Device Clinical Research job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 77% Full Time, 15% Part Time, and 7% Contract. Highlights an 89% Physical, 1% Hybrid, and 10% Remote job distribution, with an average salary of $107,336 per year, or $51.6 per hour.

Experienced Clinical Research Associate - Hematology/Oncology

Medpace, Inc.

Charlotte, NC • On-site, Remote

Other

Medical, Retirement, PTO

Re-posted 15 days ago

Medpace rating

8.6

Company rating: 8.6 out of 10

Based on 12 frontline employees who took The Breakroom Quiz

13th of 74 rated research

Job description

Job Summary
Accelerate your hematology/oncology career by joining Medpace!
This is a home-based role with excellent compensation and benefits, including an Equity/Stock option program, and additional bonus opportunities.
Medpace is growing quickly and we are seeking Experienced Clinical Research Associates to join our team. We are an innovative, scientifically oriented, mid-sized CRO focused on full-service project work. Through our expedited PACE® Training Program, you will receive customized training and efficient onboarding to familiarize yourself with Medpace systems. We also offer a certificate program (advanced training curricula) in hematology/oncology monitoring, which includes a general cancer overview, common indications, treatment options, diagnostic and reference criteria. If you're interested in expanding your therapeutic area expertise, Medpace also offers certificate programs in medical device, rare disease, infectious disease, advanced therapeutic medicinal products (ATMP), and COVID-19.
We are seeking applicants with experience in the following indications:
  • Solid Tumor
  • Breast, Ovarian, Prostate, Colorectal, Bladder, Lung, Kidney, Pancreatic Cancer
  • Small Cell Lung Cancer
  • Graft vs Host Disease
  • Glioblastoma
  • Melanoma
  • Leukemia
  • Lymphoma
  • Mesothelioma

We Offer the Following:
  • Competitive travel bonus
  • Equity/Stock option program
  • Training completion and retention bonus
  • Annual merit increases
  • 401K matching
  • 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 membership, and TSA pre-check
  • Opportunity for leadership positions - Lead CRA, CRA Manager, Training and Development Manager, and many more
  • User friendly CTMS with electronic submission and approval of monitoring visit reports;
  • Customized, expedited PACE® training program based on your experience, therapeutic background, and interest
  • Ongoing therapeutic training by our in-house physicians who are medical and regulatory experts
  • In-house administrative support for all levels of CRA
  • Opportunity 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
  • On-site and virtual/remote monitoring activities with a risk-based monitoring approach (including centralized data review) through our integrated Clinical Trial Management System to identify site deviations/deficiencies and corrective/preventive actions to bring a site back into compliance and mitigate risks moving forward
  • Verification 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
  • 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
  • Clinical Research Associate Experience (minimum 1 year), hematology/oncology exerience preferred
  • Ability to travel 60-70% to locations nationwide is required
  • Minimum of a bachelor's degree in a health or science related field
  • Proficient knowledge of Microsoft Office
  • Strong communication and presentation skills
  • Detail-oriented and efficient in time management

#LI-Remote
Medpace Overview
Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV 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 the advancement of clinical research. We leverage in-country regulatory and therapeutic expertise across all major therapeutic areas including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, we employ more than 6,500 people across 40+ countries.
Why Medpace?
When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.
Purpose-Driven Work
    • Work alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence

Collaborative Culture
    • Contribute to an interactive team environment that empowers decision making, creative thinking, and continuous learning through open communication and mutual trust.
    • Leadership throughout Medpace is both accessible and approachable

Continuous Growth & Development
    • Office based environment with on-site mentors
    • Defined career paths with clear advancement opportunities
    • Industry renowned onboarding and training programs designed to accelerate professional development
    • Ongoing training and continuous learning opportunities throughout your career
    • An environment that encourages employees to influence change, contribute ideas, and grow quickly

Other Employee Benefits
    • Competitive compensation programs that recognize and reward performance
    • Comprehensive health, wellness, retirement, and PTO benefits
    • Office based culture with occasional WFH that provides flexibility for eligible positions after training
    • Company-sponsored social events

Please note benefits may vary based on country.
What to Expect Next
A Medpace team member will review your application and if your profile matches our current needs, you will be contacted for an interview. While we review all applications carefully, we are unable to respond to every applicant, and only candidates selected for interviews will be contacted.

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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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