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Medical Device Clinical Research Manager Jobs (NOW HIRING)

Medtronic

Clinical Research Specialist

Moundsview, MN · On-site +1

Clinical trials experience within Medtronic or another medical device industry * Degree in life ... Project management experience For Baccalaureate degrees earned outside of the United States, a ...

DaVita

Regional Research Manager

Bridgeport, CT · On-site +1

Then you might be a great fit for a Clinical Studies Regional Research Manager role with DaVita ... medical device companies in the design, recruitment and completion of clinical trials using its ...

Red Nucleus

Clinical Research Scientist

Princeton, NJ · On-site

... for EU Medical Device Regulations (EU MDR). Facilitate clinical evidence reviews with cross ... Strong project management skills required, with demonstrable track record of success managing ...

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

As of Sep 2, 2026, the average yearly pay for medical device clinical research manager 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 does a medical device clinical research manager do?

A Medical Device Clinical Research Manager oversees the planning, execution, and management of clinical trials for new medical devices to ensure they meet regulatory and safety standards. They coordinate between research teams, regulatory bodies, and sponsors to ensure studies are conducted according to protocols and timelines. Their responsibilities include developing study protocols, managing budgets, ensuring data integrity, and ensuring compliance with regulatory requirements. This role is critical for bringing safe and effective medical devices to market.

What are the key skills and qualifications needed to thrive as a medical device clinical research manager?

To thrive as a Medical Device Clinical Research Manager, you need a solid background in life sciences or engineering, experience with clinical trial management, and a thorough understanding of regulatory requirements such as FDA and ISO standards. Familiarity with electronic data capture (EDC) systems, clinical trial management systems (CTMS), and certifications like ACRP or SOCRA are highly beneficial. Exceptional leadership, problem-solving, and communication skills are crucial for coordinating cross-functional teams and managing complex projects. These skills ensure compliant, efficient, and successful clinical trials that bring safe and effective medical devices to market.

What are some of the common challenges faced by medical device clinical research managers when overseeing clinical trials?

Medical Device Clinical Research Managers often encounter challenges such as ensuring compliance with complex regulatory requirements, managing timelines across multiple sites, and coordinating with diverse stakeholders including investigators, sponsors, and regulatory bodies. They must also address issues related to patient recruitment and data integrity while maintaining clear communication within cross-functional teams. Strong organizational skills and adaptability are essential to navigate these challenges and deliver successful clinical trial outcomes.
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Medical Device Clinical Research Manager jobs near you
Infographic showing various Medical Device Clinical Research Manager job openings in the United States as of August 2026, with employment types broken down into 92% Full Time, and 8% Contract. Highlights an 92% In-person, and 8% Remote job distribution, with an average salary of $107,336 per year, or $51.6 per hour.

Clinical Research Mgr

University of New Mexico

Albuquerque, NM • On-site

Full-time

Re-posted just now

University Of New Mexico rating

8.3

Company rating: 8.3 out of 10

Based on 56 frontline employees who took The Breakroom Quiz

128th of 628 rated colleges and universities

Job description

The University of New Mexico's Centerfor Memory & Aging is seeking Project Manager and Lead Research Coordinatorfor the clinical core of the newly funded New Mexico Alzheimer's Disease ResearchCenter (NM ADRC). New Mexico is joining a group of Universities across theUnited States who focus on improving research and treatment for people withAlzheimer's Disease and related Dementias. https://hsc.unm.edu/medicine/departments/neurology/research/nmadrc/  The grant is expected to be fundedthrough at least 2029.
This position is a criticallyimportant part of the Clinical Core of the NM ADRC.  The selected will work closelywith the Clinical Core Leaders and will be the lead staff member for this core.
Main responsibilities will be inoverseeing the project coordination of the local site within the grant consortium.The selected candidate will be responsible for ensuring project milestones aremet, as well as day to day coordination of the human research project. Theproject involves longitudinal study of patients with Alzheimer's disease,including collection of MRI, cognitive, neurological, blood as well as optionalstudies, including PET, CSF and add on MRI studies. This position willsupervise research coordinators as well as community health workers who workdirectly with participants.  The project also involves overseeing the coordination/managementof the clinical data collection at outlying sites including Zuni and AcomaPueblos. The clinical core collaborates closely with many other multiple coreswithin the UNM ADRC. The position may include developing or modifying IRBdocuments for submission to the HRPO (IRB), or work closely with other stafffor these documents. Position may require occasional out of state travel tonational meetings, as well as occasional travel to the Zuni Pueblo or otherlocations within NM.
Additional responsibilities will include working as backupresearch coordinator and may include a cohort of participants for ongoingresearch studies, which includes recruiting, scheduling and screening patients,conducting assessments, ensuring protocol adherence for each specified study,and maintaining accurate records.  Dutiesalso include the collection, compilation, and management of study data andreview of patient records for past and present health issues. Weekly consensusdiagnosis meetings will be coordinated by this position in conjunction with theother core contributions.
The individual in this positionmust have strong interpersonal and communication skills and the ability to workeffectively with a wide range of people in a diverse community, particularlyolder adults with cognitive difficulties and their families. This position alsorequires a person with professional presentation and interpersonal skills. Theselected person must be adept at organization and project management. Thisemployee will work with confidential information and data, work directly withpatients, schedule and coordinate research appointments and examinations.Position may also include other clinical assessments, such as drawing andprocessing of blood samples, ECGs, vitals.

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