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Medical Device Clinical Research Project Manager Jobs

DaVinci Research

Clinical Research Coordinator

Roseville, CA · On-site

$25.50 - $33.75/hr

... Management Organization dedicated to conducting clinical research trials. In collaboration with innovative pharmaceutical and medical device companies worldwide, DVR serves as a bridge between ...

Abbott

Clinical Research Associate II

Alameda, CA · On-site

$81K - $141K/yr

Conduct single or multi-center medical device clinical studies. * Perform study site visits (SQV ... Able to manage numerous projects/conflicting priorities, and to be flexible when priorities change.

Abbott

Clinical Research Associate II

Alameda, CA · On-site

Conduct single or multi-center medical device clinical studies. * Perform study site visits (SQV ... Able to manage numerous projects/conflicting priorities, and to be flexible when priorities change.

Abbott

Clinical Research Associate II

Alameda, CA

Conduct single or multi-center medical device clinical studies. * Perform study site visits (SQV ... Able to manage numerous projects/conflicting priorities, and to be flexible when priorities change.

Veranex

Sr Clinical Research Associate

Raleigh, NC · On-site

$98K - $140K/yr

... the medical device industry. Our team supports start-ups, mid-sized private companies, and the ... Must have strong project management competencies and ability to work with high quality, reliability ...

Iowa State University

Research Project Manager

Ames, IA · On-site

$69K - $89K/yr

Research Project Manager Job Group: Professional & Scientific Required Minimum Qualifications ... Iowa State Employees enjoy comprehensive health and work-life benefits, including medical and ...

Kelly Services

Clinical Research Specialist

Irvine, CA · On-site

... management level. Function as a reliable, trusted resource of accurate, up-to-date project ... Medical device experience is a plus REQUIRED KNOWLEDGE, SKILLS, ABILITIES, CERTIFICATIONS/LICENSES ...

Baylor Scott & White Health

Research Project Manager

Plano, TX · On-site

$66K - $85K/yr

Provides input to the Principal Investigator on clinical and research issues to establish financial ... Ability to manage time-reactive projects. * Knowledge of the beliefs and practices of developing ...

Hub Technology Group

Research Project Manager

Boston, MA · Hybrid

$65 - $80/hr

1 Year+ Project - HYBRID IN BOSTON - Must Be Local - Must be W2 5+ Years of Project Management Experiece Required 2+ Years of experience working with Researchers & Scientists Familiarity with Linux ...

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Medical Device Clinical Research Project Manager information

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

As of Sep 9, 2026, the average hourly pay for medical device clinical research project manager in the United States is $60.70, according to ZipRecruiter salary data. Most workers in this role earn between $42.31 and $71.15 per hour, depending on experience, location, and employer.

What are popular job titles related to Medical Device Clinical Research Project Manager jobs?

For Medical Device Clinical Research Project Manager jobs, the most frequently searched job titles are:

Infographic showing various Medical Device Clinical Research Project Manager job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 14% Part Time, and 6% Contract. Highlights an 87% Physical, 1% Hybrid, and 12% Remote job distribution, with an average salary of $126,262 per year, or $60.7 per hour.

Clinical Project Manager

Minnetonka, MN

Laborie Medical Technologies Corp
Retail • 501 - 1,000 employees
Learn more about Laborie Medical Technologies Corpexternal

$130K - $135K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 11 days ago

Key responsibilities

  • Manage all aspects of Clinical Trial Team activities for assigned projects, including trial timeline, budget, resources, and vendors.

  • Lead sponsor study startup processes such as conducting kick-off meetings, setting up trial master files, and finalizing site and vendor agreements.

  • Monitor vendor deliverables, address quality issues, and ensure all project documentation is filed in accordance with SOPs and regulatory requirements.

Job description

We believe that great healthcare is an essential safeguard of human dignity.
At Laborie, we know the work we do matters – it’s what fuels our motivation and contributes to our success. If you’re ready to make a positive impact in the lives of patients across the globe, we’d like to meet you.
 
We support and empower our employees to grow their careers in an environment that encourages a sense of belonging and a connection to doing good. We’re not afraid to roll up our sleeves to make our goals a reality and work together to solve for our customers. We reward and recognize our employees based on our values of Aspire to Greatness, Respect All, Own It, Working Together, Persist with Passion.
 
Who We’re Looking For:
As a key member of the Clinical team, the Clinical Project Manager (CPM) is responsible for the management of all aspects of Clinical Trial Team activities for assigned project(s). The CPM, in concert with the Clinical Program Manager, is accountable for achieving successful delivery of Laborie Clinical Team activities at the project level by meeting company and regulatory requirements according to time, quality/scope, and budget constraints.  
 
About the Role:
  • Proactively manage project level operational aspects of Clinical Research Team (CRT) including management of trial timeline, budget, resources, and vendors.
  • Provide efficient updates on trial progress to the Clinical Program Manager and/or Chief Technology Officer, with respect to vendor selection, project plans, trial budget and timeline management, quality standards and risk mitigation.
  • Lead sponsor study startup process, including but not limited to conduct of the Trial Kick-off meeting, the setup of trial master file (TMF), site selection and finalization of site and vendor Clinical Trial Agreements and budgets.
  • Ensure effective project plans are in place and operational for each trial and work proactively with the Clinical Research Team to set priorities in accordance with applicable project plans, company standard operational procedures (SOPs), ICH/GCP guidelines and regulatory requirements.
  • Chair Clinical Research Team working group and vendor status update meetings and ensure meeting minutes are completed, distributed to team members, and filed in the Trial Master File (TMF) in a timely manner.
  • Monitor the quality of vendor deliverables, address quality issues with the appropriate team member and identify opportunities to improve training, execution, and quality control across the clinical team.
  • Review and approve vendor invoices in collaboration with the accounting team to ensure investigator payments occur in a timely manner.
  • Ensure all project level study documentation is filed in the TMF in accordance with company SOPs/all regulatory requirements and provide oversight to the clinical team regarding TMF filing, maintenance and archival procedures 
  • Effectively provide support to the Clinical Research Team in the conduct of the trial(s). 
Minimum Qualifications:
  • Bachelor's degree in Life Sciences; Master's or Doctoral degree preferred.
  • 8+ years of clinical operations experience for CPM; with increasing levels of responsibility in the medical device or CRO industry is required.
  • Minimum 2 years of clinical project management experience at a sponsor or CRO company is preferred.
  • Therapeutic/intervention experience in urogynecology, gastroenterology, and/or OB/GYN.
  • Experience with medical devices CER, PMS, PMCF, PSUR medical writing.
  • Speak fluent English, excellent verbal and written communication skills, Microsoft Office, Excel, PowerPoint, Outlook, Teams, etc.
  • Must have thorough knowledge of clinical research concepts, practices, and FDA/EU regulations and ICH Guidelines, ISO 14155, clinical research, and data management methods.  
Why Laborie:
Our Mission every day is to operate as a world-class specialist medical company making and advancing technologies that preserve and restore human dignity. We do that today by helping people with pelvic and gastrointestinal conditions live normal lives, and by helping mothers and babies have safe deliveries.
  • Paid time off and paid volunteer time
  • Medical, Dental, Vision and Flexible Spending Account
  • Health Savings Account with Company Funded Contributions
  • 401k Retirement Plan with Company Match
  • Parental Leave and Adoption Services
  • Health and Wellness Programs and Events
  • Awarded 2025 Cigna Healthy Workforce Designation Gold Level
Laborie provides equal employment opportunities and non-discrimination for all employees and qualified applicants without regard to a person’s race, color, gender, age, religion, national origin, ancestry, disability, veteran status, genetic information, sexual orientation, or any characteristic protected under applicable law. Laborie is committed to providing access and reasonable accommodation in our services, activities, education, and employment for individuals with disabilities.