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Medical Device Clinical Research Manager Jobs in Rochester, NY

Clinical Research Coordinator Location: Rochester, NY Type: Contract Compensation: $26.00 - $30.00 ... Medical terminology & patient care experience required. * Strong organizational, time management ...

Clinical Research Coordinator Location: Rochester, NY Type: Contract thru end of year with ... Medical terminology & patient care experience required. * Strong organizational, time management ...

Clinical Research Coordinator Location: Rochester, NY Type: Contract Compensation: $26.00 - $30.00 ... Medical terminology & patient care experience required. * Strong organizational, time management ...

Clinical Research Coordinator Location: Rochester, NY Type: Contract Compensation: $26.00 - $30.00 ... Medical terminology & patient care experience required. * Strong organizational, time management ...

Clinical Research Coordinator Location: Rochester, NY Type: Contract Compensation: $26.00 - $30.00 ... Medical terminology & patient care experience required. * Strong organizational, time management ...

Clinical Research Coordinator Location: Rochester, NY Type: Contract Compensation: $26.00 - $30.00 ... Medical terminology & patient care experience required. * Strong organizational, time management ...

Clinical Research Coordinator Location: Rochester, NY Type: Contract Compensation: $26.00 - $30.00 ... Medical terminology & patient care experience required. * Strong organizational, time management ...

Clinical Research Coordinator Location: Rochester, NY Type: Contract Compensation: $26.00 - $30.00 ... Medical terminology & patient care experience required. * Strong organizational, time management ...

Clinical Research Nurse Location: Rochester, NY Type: Contract To Hire Compensation: $40.00 - $50 ... medical research and making a positive impact on patient outcomes. Responsibilities * Manage all ...

Clinical Research Nurse Location: Rochester, NY Type: Contract To Hire Compensation: $40.00 - $50 ... medical research and making a positive impact on patient outcomes. Responsibilities * Manage all ...

Clinical Research Nurse Location: Rochester, NY Type: Contract To Hire Compensation: $40.00 - $50 ... medical research and making a positive impact on patient outcomes. Responsibilities * Manage all ...

Manage all aspects of a study ensuring adherence to the protocol, GCP, and applicable regulations ... medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as ...

Manage all aspects of a study ensuring adherence to the protocol, GCP, and applicable regulations ... medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as ...

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Showing results 1-20

Medical Device Clinical Research Manager information

See Rochester, NY salary details

$48.3K

$105.9K

$186.5K

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

As of Sep 1, 2026, the average yearly pay for medical device clinical research manager in Rochester, NY is $105,905.00, according to ZipRecruiter salary data. Most workers in this role earn between $79,900.00 and $120,900.00 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.

What are the most commonly searched types of Medical Device Clinical Research jobs in Rochester, NY?

The most popular types of Medical Device Clinical Research jobs in Rochester, NY are:

What are popular job titles related to Medical Device Clinical Research Manager jobs in Rochester, NY?

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

What job categories do people searching Medical Device Clinical Research Manager jobs in Rochester, NY look for?

The top searched job categories for Medical Device Clinical Research Manager jobs in Rochester, NY are:

What cities near Rochester, NY are hiring for Medical Device Clinical Research Manager jobs?

Cities near Rochester, NY with the most Medical Device Clinical Research Manager job openings:

Infographic showing various Medical Device Clinical Research Manager job openings in Rochester, NY as of August 2026, with employment types broken down into 100% Full Time. Highlights an 87% In-person, and 13% Remote job distribution, with an average salary of $105,905 per year, or $50.9 per hour.

Clinical Supply Manager

Kelly Services

Rochester, NY

$47/hr

Full-time

Medical, Dental, Vision, Life, Retirement

Re-posted 5 days ago


Job description

Kelly Science & Clinical has a new, temporary opportunity for a Clinical Supply Manager in Rochester, NY!
Shift: Monday – Friday 8am-5pm
A 4 month temporary opportunity with possibility to extend into 2027
Pay: $47/hour
Hybrid Flexibility
Objective:
Supply chain management through sourcing, packaging, labelling, inventory control, temperature control, and global distribution and return of the clinical supplies.
Responsibilities:
  • Work with functional teams to develop clinical protocol.
  • Plan and procure clinical supplies for pharmaceutical and medical device clinical studies.
  • Clinical Supply Plan development; trial characteristics, study materials, treatment groups, packaging design, label text, distribution strategy.
  • Internal coordination of secondary labeling, packaging, inventory, and depot distribution of clinical supplies.
  • Work with external vendors for clinical labeling, packaging, and distribution.
  • Development and collaboration with Clinical Ops, Regulatory and Translation services of label copy requirements for clinical materials.
  • Collaborate with Statisticians and Data Management for clinical supply randomization kit/med list.
  • Collaborate with Clinical Ops and Data Management for RTSM system set-up. UAT testing.
  • Manage Vendor POs.
  • Budgeting/Forecasting Clinical Supply spend.
  • Laboratory Control and Compliance Team member.
  • Clinical Supply SOP creation and maintenance.
  • Reconciliation and destruction of clinical trial study supplies.

Key Relationships:
  • Internal customers to include Clinical Operations, Data Management, Statistics, Medical Affairs, Regulatory, Quality, Procurement, and Engineers. External customers/partners to include, Clinical Research Organizations, IP Manufacturers (CMOs), and Clinical Labeling & Packaging vendors.

Qualifications:
  • Bachelor’s degree, interpersonal skills, multi-task, understanding of clinical trial procedures, work in fast-paced environment.
  • 5+ years of relevant project management experience, given preference
  • Exemplary organizational and time management skills
  • Excellent verbal and written communication skills
If you, or someone you know would like to be considered for this opportunity, please apply online today to discuss the next steps.
 
As part of our promise to talent, Kelly supports those who work with us through a variety of benefits, perks, and work-related resources. Kelly offers eligible employees voluntary benefit plans including medical, dental, vision, telemedicine, term life, whole life, accident insurance, critical illness, a legal plan, and short-term disability. As a Kelly employee, you will have access to a retirement savings plan, service bonus and holiday pay plans (earn up to eight paid holidays per benefit year), and a transit spending account. In addition, employees are entitled to earn paid sick leave under the applicable state or local plan. Click here for more information on benefits and perks that may be available to you as a member of the Kelly Talent Community.

Why Kelly® Science & Clinical?

Kelly Science & Clinical is your connection to premier scientific and clinical companies looking to hire industry experts just like you. Our team creates expert talent solutions to solve the world’s most critical challenges. Every day, we match science professionals with dream jobs that fit their skills, interests, and career goals-it’s the way we think job searching should be. Nearly 100 percent of our science recruiters have a professional background and education in science, so we know a thing or two about the science market and how to get your expertise noticed.

About Kelly

Work changes everything. And at Kelly, we’re obsessed with where it can take you. To us, it’s about more than simply accepting your next job opportunity. It’s the fuel that powers every next step of your life. It’s the ripple effect that changes and improves everything for your family, your community, and the world. Which is why, here at Kelly, we are dedicated to providing you with limitless opportunities to enrich your life-just ask the 300,000 people we employ each year.
Kelly is committed to providing equal employment opportunities to all qualified employees and applicants regardless of race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or any other legally protected status, and we take affirmative action to recruit, employ, and advance qualified individuals with disabilities and protected veterans in the workforce. Requests for accommodation related to our application process can be directed to the Kelly Human Resource Knowledge Center. Kelly complies with the requirements of California’s state and local Fair Chance laws. A conviction does not automatically bar individuals from employment. Kelly participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S.
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