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Medical Device Clinical Research Jobs (NOW HIRING)

Red Nucleus

Clinical Research Scientist

Princeton, NJ · On-site

$110 - $160/hr

The Clinical Research Scientist will be responsible for the development of post-market clinical ... for EU Medical Device Regulations (EU MDR). Facilitate clinical evidence reviews with cross ...

WHOOP

Director, Clinical Operations

Boston, MA · On-site

$210 - $230/hr

Strong understanding of GCP, FDA regulations, ISO 14155, IRB/Ethics Committee processes, and medical device clinical research requirements. * Excellent written and verbal communication skills, with ...

Red Nucleus

Clinical Research Scientist

Princeton, NJ · On-site

The Clinical Research Scientist will be responsible for the development of post-market clinical ... for EU Medical Device Regulations (EU MDR). Facilitate clinical evidence reviews with cross ...

Rednucleus

Clinical Research Scientist

Princeton, NJ · On-site

The Clinical Research Scientist will be responsible for the development of post-market clinical ... for EU Medical Device Regulations (EU MDR). Facilitate clinical evidence reviews with cross ...

Catholic Health

Research Coordinator

Roslyn, NY · On-site

$32 - $50/hr

Job Details The Research Coordinator is responsible for coordinating and managing clinical research ... medical device clinical trials by attending study start-up meetings, summarizing protocols, and ...

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Medical Device Clinical Research information

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

As of Sep 3, 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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Cities with the most Medical Device Clinical Research job openings:

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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.

Clinical Research Scientist

Red Nucleus

Princeton, NJ • On-site

$110 - $160/hr

Other

This job post has expired today. Applications are no longer accepted.

Job description

The Clinical Research Scientist will be responsible for the development of post-market clinical research strategies of orthopedic devices to support global regulatory and post-market surveillance requirements.

Responsibilities include:

  • Work closely with cross-functional teams (Clinical, Medical, Regulatory, R&D, Marketing) to develop post market clinical evidence generation strategies that consider evidence needs for EU Medical Device Regulations (EU MDR). Facilitate clinical evidence reviews with cross functional team to align clinical evidence strategies, document / track decisions and risks, and write PMCF Plans.
  • Develop and write high quality Post-market Clinical Follow-up (PMCF) plans and reports with minimal supervision. Support development and drafting of clinical study protocols, registry plans, epidemiology studies, informed consents, investigator brochures, and other study materials where needed.
  • Review summaries of clinical evidence and PMCF strategies in other areas of the Technical Documentation for accuracy and completeness. This includes the Clinical Evaluation Plan, Clinical Evaluation Report (CEP), Post Market Surveillance Plan and Periodic Safety Update Report (PSUR).
  • Where required, foster relationships with surgeons, hospitals and research teams to gain input into study design, evaluate study feasibility, and identify sites for study execution or data collection. Develop strong collaborative relationships with the study core team and others to ensure study progress for assigned projects and that issues are identified and communicated to leaders.
  • Partner with the Contracts and Payments team to ensure timely execution of all study agreements and corresponding payments for achieved milestones and deliverables.
  • Support clinical scientific discussions with internal stakeholders within Clinical, Medical, Regulatory, R&D and Marketing to drive support of the clinical and regulatory strategy, communicate evidence needs.
  • Contribute to appropriate interpretation and dissemination of all evidence generated, including abstracts, manuscripts, and Clinical Study Reports (CSR), epidemiology study results and clinical literature.
  • Develop a strong understanding of the orthopedic device product portfolio and business needs for clinical evidence to meet regulatory requirements.
Qualifications
  • A Master’s degree in Biological Science or related discipline, with a minimum of 4 years’ experience in the medical device industry or healthcare field is required
  • Advanced technical writing skills is required, with demonstrated experience in writing PMCF plans / reports strongly preferred.
  • Clinical expertise in the medical device sector
  • Proven experience in conducting clinical studies, registries particularly in the field of orthopaedics
  • Strong project management skills required, with demonstrable track record of success managing multiple projects simultaneously with minimal supervision.
  • Excellent communication skills, including effective interaction with healthcare professionals (HCPs), hospital staff etc.

Diversity, equity and inclusion are valued at Red Nucleus and we believe we have a shared responsibility to provide equal opportunity and foster an inclusive spirit. We do not discriminate on the basis of race, color, national origin, religion, caste, sexual orientation, gender, age, marital status, veteran status, or disability status.

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