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Clinical Trials Jobs in Rochester, NY (NOW HIRING)

Research RN

Rochester, NY · On-site

$35.35 - $47.72/hr

Reports to the Manager of the Cardiology Clinical Trials Unit ESSENTIAL FUNCTIONS * Coordinates the administrative details required to initiate and conduct human subject research, such as, receiving ...

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Clinical Trials information

See Rochester, NY salary details

$28

$61

$94

How much do clinical trials jobs pay per hour?

As of Aug 21, 2026, the average hourly pay for clinical trials in Rochester, NY is $61.68, according to ZipRecruiter salary data. Most workers in this role earn between $50.05 and $69.47 per hour, depending on experience, location, and employer.

What is a clinical trial?

A Clinical Trials job involves managing, coordinating, or supporting research studies that evaluate the safety and effectiveness of medical treatments, drugs, or devices. Professionals in this field work on trial design, patient recruitment, data collection, regulatory compliance, and reporting results. Roles can range from clinical research coordinators to trial managers and regulatory specialists. The goal is to ensure that studies follow ethical guidelines and produce reliable data for medical advancements.

What are some common career paths or advancement opportunities for professionals working in clinical trials?

Many professionals in Clinical Trials start their careers as Clinical Research Coordinators, Clinical Research Associates, or Data Managers. With experience, you can advance to roles such as Senior Clinical Research Associate, Clinical Trial Manager, or Project Manager, and potentially move into areas like regulatory affairs, medical writing, or quality assurance. The role offers continuous learning opportunities, exposure to innovative therapies, and often provides the chance to lead larger, more complex studies as you progress. Advancement is typically supported by additional certifications, strong performance, and a proactive approach to professional development. Teamwork and networking within the industry can also open new doors for growth.

What are the key skills and qualifications needed to thrive in a clinical trials position, and why are they important?

To thrive in Clinical Trials roles, you need a strong understanding of clinical research principles, Good Clinical Practice (GCP) guidelines, and a background in life sciences or healthcare. Familiarity with electronic data capture (EDC) systems, regulatory compliance software, and relevant certifications such as GCP or CCRA is highly valuable. Attention to detail, organizational skills, and effective communication enable collaboration across multidisciplinary teams. These competencies are crucial for ensuring protocol adherence, data integrity, and the successful execution of trial activities.

What are the most commonly searched types of Clinical Trials jobs in Rochester, NY?

The most popular types of Clinical Trials jobs in Rochester, NY are:

What are popular job titles related to Clinical Trials jobs in Rochester, NY?

For Clinical Trials jobs in Rochester, NY, the most frequently searched job titles are:

What cities near Rochester, NY are hiring for Clinical Trials jobs?

Cities near Rochester, NY with the most Clinical Trials job openings:

Infographic showing various Clinical Trials job openings in Rochester, NY as of August 2026, with employment types broken down into 3% As Needed, 70% Full Time, 18% Part Time, and 9% Contract. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $128,301 per year, or $61.7 per hour.

Sr. Clinical Trials Project Manager

University of Rochester

Rochester, NY • On-site

$70.60 - $105.80/hr

Other

Posted 3 days ago

New


University Of Rochester rating

8.3

Company rating: 8.3 out of 10

Based on 186 frontline employees who took The Breakroom Quiz

126th of 620 rated colleges and universities


Job description

## Sr. Clinical Trials Project ManagerApplyremote type: Hybridlocations: Saunders Research Buildingtime type: Full timeposted on: Posted Todayjob requisition id: R273180As a community, the University of Rochester is defined by a deep commitment to Meliora - Ever Better. Embedded in that ideal are the values we share: equity, leadership, integrity, openness, respect, and accountability. Together, we will set the highest standards for how we treat each other to ensure our community is welcoming to all and is a place where all can thrive.**Job Location (Full Address):**265 Crittenden Blvd, Rochester, New York, United States of America, 14642**Opening:**Worker Subtype:RegularTime Type:Full timeScheduled Weekly Hours:40Department:400981 Neuro-Ctr Health & Tech/CTCCWork Shift:UR - Day (United States of America)Range:UR URG 112Compensation Range:$70,600.00 - $105,800.00*The referenced pay range represents the minimum and maximum compensation for this job. Individual annual salaries/hourly rates will be set within the job's compensation range, and will be determined by considering factors including, but not limited to, market data, education, experience, qualifications, expertise of the individual, and internal equity considerations.***Responsibilities:**Directs and coordinates all aspects of clinical research trials and acts as a liaison to study leadership and sponsor(s). Ensures study activities are meeting deadlines and manages overall study timeline. Provides oversight and mentoring to junior members of the study team.**ESSENTIAL FUNCTIONS*** Directs the development and execution of clinical trial activities for multi-center industry sponsored drug trials, including developing and revising study timelines. Engages with Finance for budget development and budget management.* Serves as liaison to the Principal Investigator, study leadership, sites, vendors and sponsor. Helps coordinate work between entire study team, including clinical trial sites, clinical and research laboratories, study medical monitors, biostatistics core, and data management team. Represents study team in meetings and during training sessions with sites.* Leads internal study meetings and monitors progress toward meeting team goals and completing action items. Participates in planning external meetings, including development of agenda and meeting materials and may be required to present or report out on action items.* Mentors, trains, and manages more junior staff as part of a study project team. Provides professional direction within clinical trials coordination team. Oversees study team interactions with study sites.* Drafts and/or completes internal review of study documents, such as protocols, amendments, study plans, DSMB reports, grant submissions, and annual reports, for review and approval by study leadership. Drafts requests and reports to regulatory agencies, such as IND application, annual IND update to FDA, etc.* Reviews monitoring reports and works with study monitors to finalize reports. Manages monitoring schedule in coordination with the monitoring team.* Presents at larger scale external meetings, and well as other professional meetings.* Other duties as assigned.**MINIMUM EDUCATION & EXPERIENCE*** Bachelor's degree and 5 years of relevant experience required* Master's degree preferred* Or equivalent combination of education and experience* Previous personnel/study team management experience preferred**KNOWLEDGE, SKILLS AND ABILITIES*** Clinical trials project management experience including extensive knowledge of protocol planning, implementation, coordination, evaluation, and reporting of clinical trials required* Strong communication skills, interpersonal skills, attention to detail, and organization skills required**LICENSES AND CERTIFICATIONS*** CCRP - Certified Clinical Research Professional upon hire referred* Certified Project Management Professional (PMP)-PMI upon hire preferredpThe University of Rochester is committed to fostering, cultivating, and preserving an inclusive and welcoming culture to advance the University’s Mission to Learn, Discover, Heal, Create – and Make the World Ever Better. In support of our values and those of our society, the University is committed to not discriminating on the basis of age, color, disability, ethnicity, gender identity or expression, genetic information, marital status, military/veteran status, national origin, race, religion, creed, sex, sexual orientation, citizenship status, or any other characteristic protected by federal, state, or local law (Protected Characteristics). This commitment extends to non-discrimination in the administration of our policies, admissions, employment, access, and recruitment of candidates, for all persons consistent with our values and based on applicable law. #J-18808-Ljbffr

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