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Clinical Research Project Manager Jobs in Rochester, NY

Datrose, Inc

Clinical Research Nurse

Rochester, NY · On-site

$45/hr

The Clinical Research Nurse will support on-going multi-year projects related to electronic ... Additional responsibilities relate to research study management, including submitting IRB and ...

Datrose

Clinical Research Nurse

Rochester, NY

$45/hr

The Clinical Research Nurse will support on-going multi-year projects related to electronic ... Additional responsibilities relate to research study management, including submitting IRB ...

Datrose

Clinical Research Nurse

Rochester, NY

$45/hr

The Clinical Research Nurse will support on-going multi-year projects related to electronic ... Additional responsibilities relate to research study management, including submitting IRB ...

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Clinical Research Project Manager information

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$49.3K

$84.9K

$130.2K

How much do clinical research project manager jobs pay per year?

As of May 28, 2026, the average yearly pay for clinical research project manager in Rochester, NY is $84,885.00, according to ZipRecruiter salary data. Most workers in this role earn between $70,500.00 and $90,300.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Clinical Research Project Manager, and why are they important?

To thrive as a Clinical Research Project Manager, you need a solid background in clinical research, project management, and regulatory compliance, typically supported by a degree in life sciences or a related field. Familiarity with tools such as CTMS (Clinical Trial Management Systems), EDC (Electronic Data Capture), and certifications like PMP or ACRP-PM is highly valuable. Strong leadership, communication, and problem-solving skills help you coordinate teams and manage stakeholder expectations. These competencies are crucial to ensure trials are conducted efficiently, ethically, and in line with regulatory standards.

What are some common challenges faced by Clinical Research Project Managers and how can they be addressed?

Clinical Research Project Managers often encounter challenges such as managing complex timelines, ensuring regulatory compliance, and coordinating communication between diverse stakeholders. Balancing the needs of sponsors, research teams, and regulatory bodies requires strong organizational and problem-solving skills. Staying proactive with risk management and fostering clear, consistent communication can help address these challenges effectively. Leveraging project management tools and regularly scheduled check-ins also supports smoother project execution and team collaboration.

What does a Clinical Research Project Manager do?

A Clinical Research Project Manager oversees the planning, execution, and management of clinical research studies. They coordinate teams, ensure regulatory compliance, manage budgets and timelines, and act as a liaison between stakeholders such as sponsors, investigators, and regulatory agencies. Their primary goal is to ensure that clinical trials are conducted efficiently, ethically, and according to protocol. This role requires strong organizational, leadership, and communication skills, as well as a deep understanding of clinical research processes.

What is the difference between Clinical Research Project Manager vs Clinical Research Coordinator?

AspectClinical Research Project ManagerClinical Research Coordinator
CredentialsBachelor's or higher in life sciences, often with project management certificationsBachelor's in health sciences or related field, often with clinical research certifications
Work EnvironmentOversees multiple projects, manages teams, and liaises with sponsorsConducts daily clinical trial activities, interacts directly with participants and site staff
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsResearch hospitals, clinics, academic institutions

The Clinical Research Project Manager focuses on overseeing entire clinical trials, managing teams, and ensuring project milestones are met. In contrast, the Clinical Research Coordinator handles the day-to-day activities at trial sites, ensuring protocol adherence and participant safety. Both roles are essential but differ in scope and responsibilities.

What are the most commonly searched types of Clinical Research Project jobs in Rochester, NY? The most popular types of Clinical Research Project jobs in Rochester, NY are:
What are popular job titles related to Clinical Research Project Manager jobs in Rochester, NY? For Clinical Research Project Manager jobs in Rochester, NY, the most frequently searched job titles are:
What job categories do people searching Clinical Research Project Manager jobs in Rochester, NY look for? The top searched job categories for Clinical Research Project Manager jobs in Rochester, NY are:
What cities near Rochester, NY are hiring for Clinical Research Project Manager jobs? Cities near Rochester, NY with the most Clinical Research Project Manager job openings:
Clinical Research Project Manager jobs near you
Infographic showing various Clinical Research Project Manager job openings in Rochester, NY as of May 2026, with employment types broken down into 80% Full Time, 8% Part Time, and 12% Contract. Highlights an 92% In-person, and 8% Remote job distribution, with an average salary of $84,885 per year, or $40.8 per hour.
Clinical Research Nurse

Clinical Research Nurse

Datrose, Inc

Rochester, NY • On-site

$45/hr

Full-time

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

Job description

Job description
**Immediate Interviews**
Our client is Rochester Institute of Technology. This is a 6-month maximum contract ON-SITE with opportunity to become hired full-time, with pay starting at $45/hour.
Position Summary:
The Clinical Research Nurse will support on-going multi-year projects related to electronic cigarette use. The primary focus will be on the execution of study protocols by performing clinical tasks such as bio-sample collection (saliva, urine, blood), preparation, and storage, as well as participant care insofar as adverse event tracking and contingency planning. Additional responsibilities relate to research study management, including submitting IRB and Institutional Biosafety Committee (IBC) application and obtaining approval, participant recruitment, education, and oral and written communication; weekly updates at team meetings, data collection, storage, preparation, and analysis.
30 to 40 hrs. per week, 8 am to 5 pm typical, flexible work hours, swapping weekdays for weekends and evenings.
Essential Tasks:
Primary responsibilities include, but are not limited to:
Conducting and supporting participant visits (data and bio-sample collection)
Reviewing study procedures to ensure compliance with GCP and general good medical practice
Participant recruitment including outreach and candidate tracking
Study data tracking, storage, preparation, and analysis
Preparation of process documentation
Team communication (answering technical questions, debriefing technical processes, meetings)
Qualifications/Special Skills Required:
Certification, professional license, or credential:
NCLEX-RN certification required (registered nurse)
3 years nursing experience
Computer literacy including spreadsheets, power-point, adobe pdf, slack
Valid driver's license (indicate required class): regular passenger vehicles
The position does not have any regular responsibility for overseeing or supervising the work of other employees.

#IND-1
Datrose is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race. Religion, color, national origin, sexual orientation, gender identity, pregnancy, status as a parent, age, protected veteran status, family medical history or genetic information, political affiliation, status as a qualified individual with disability, or other non-merit-based factors.
Authorization to work in the U.S. is a precondition of employment. Datrose does not sponsor employment visas.