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Clinical Research Study Jobs in Rochester, NY (NOW HIRING)

System One

Registered Dietitian

Rochester, NY · On-site

$45 - $50/hr

In this role, you'll combine your nutrition expertise with clinical research responsibilities, working directly with study participants through counseling visits, study screenings, and ongoing trial ...

410 ICR United States USA

Senior CRA

Rochester, NY · On-site

$110K - $138K/yr

Senior CRA- Phase I Oncology/NY/NJ ICON is a global healthcare intelligence and clinical research ... Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements ...

ICON

Senior CRA- Phase I Oncology- NY/NJ/PA

Rochester, NY · On-site +1

$110K - $138K/yr

Senior CRA- Phase I Oncology/NJ/NY ICON is a global healthcare intelligence and clinical research ... Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements ...

ICON

Senior CRA- Phase I Oncology- NJ/NY

Rochester, NY · On-site +1

$110K - $138K/yr

Senior CRA- Phase I Oncology/NY/NJ ICON is a global healthcare intelligence and clinical research ... Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements ...

410 ICR United States USA

Senior CRA

Rochester, NY

$110K - $138K/yr

Senior CRA- Phase I Oncology/NJ/NY ICON is a global healthcare intelligence and clinical research ... Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements ...

ICON

Senior CRA- Phase I Oncology- NY/NJ/PA

Rochester, NY · On-site +1

$110K - $138K/yr

Senior CRA Phase I Oncology- NY/NJ ICON is a global healthcare intelligence and clinical research ... Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements ...

410 ICR United States USA

Senior CRA

Rochester, NY · On-site

$110K - $138K/yr

Senior CRA Phase I Oncology- NY/NJ ICON is a global healthcare intelligence and clinical research ... Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements ...

University of Rochester

Research RN

Rochester, NY · On-site

$35.35 - $47.72/hr

Typical duties will include but are not limited to evaluating study protocols regarding standard of care and research-oriented tasks, evaluating time effort needed to complete clinical tasks and ...

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Clinical Research Study information

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How much do clinical research study jobs pay per hour?

As of Aug 6, 2026, the average hourly pay for clinical research study in Rochester, NY is $23.77, according to ZipRecruiter salary data. Most workers in this role earn between $19.90 and $24.42 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in clinical research studies, and why are they important?

To thrive in clinical research studies, you need a background in life sciences or healthcare, strong analytical skills, and knowledge of research methodologies, often supported by a degree in a related field. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and Good Clinical Practice (GCP) certification is typically required. Attention to detail, strong organizational skills, and effective communication are crucial soft skills for managing protocols, collaborating with teams, and maintaining regulatory compliance. These competencies ensure the integrity of research data, patient safety, and the successful execution of clinical trials.

What qualifications do you need to be a clinical research study?

A clinical research study is not a job but a type of research; however, professionals involved typically need a relevant degree in healthcare, life sciences, or a related field, along with knowledge of Good Clinical Practice (GCP) guidelines and regulatory requirements. Skills in data collection, patient interaction, and familiarity with clinical trial protocols are also important. Certification such as Certified Clinical Research Professional (CCRP) can enhance qualifications.

What are some common challenges faced by professionals working in clinical research studies, and how can they be addressed?

Professionals involved in clinical research studies often face challenges such as patient recruitment, maintaining regulatory compliance, and ensuring accurate data collection. Recruitment can be difficult due to strict inclusion criteria or participant hesitancy, but building partnerships with healthcare providers and clear communication can help. Staying updated on regulatory requirements and utilizing electronic data capture systems can streamline compliance and data accuracy. Effective teamwork and regular communication with investigators, coordinators, and sponsors are essential for addressing these challenges and ensuring study success.

What is a clinical research study?

A clinical research study is a scientific investigation involving human participants, designed to evaluate medical, surgical, or behavioral interventions. These studies help determine the safety and effectiveness of new treatments, drugs, medical devices, or procedures. Clinical research can include clinical trials, observational studies, and longitudinal studies. Participation is usually voluntary, and studies are conducted under strict ethical guidelines to protect participants' rights and safety.

What is the difference between Clinical Research Study and Clinical Research Coordinator?

AspectClinical Research StudyClinical Research Coordinator
RoleParticipates in designing, conducting, and analyzing clinical trialsManages daily trial operations, patient recruitment, and data collection
Required CredentialsOften requires clinical research training, degrees in health sciences, or related certificationsTypically requires similar certifications, with additional experience in patient interaction
Work EnvironmentResearch labs, hospitals, or clinical trial sitesClinical trial sites, hospitals, or research facilities
Employer & Industry UsagePharmaceutical companies, CROs, academic institutionsHospitals, research organizations, pharmaceutical companies

While a Clinical Research Study involves designing and analyzing trials, a Clinical Research Coordinator focuses on managing trial operations and patient interactions. Both roles require similar credentials and work in related environments, but their responsibilities differ significantly.

What can I do with a clinical research study degree?

A degree related to clinical research studies prepares individuals for roles such as clinical research coordinator, data manager, or regulatory specialist. These positions involve managing clinical trials, ensuring compliance with protocols, and working with research teams using tools like electronic data capture systems. Opportunities exist in pharmaceutical companies, research institutions, and healthcare organizations.
What are the most commonly searched types of Clinical Research Study jobs in Rochester, NY? The most popular types of Clinical Research Study jobs in Rochester, NY are:
Clinical Research Study jobs near you
Infographic showing various Clinical Research Study job openings in Rochester, NY as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $49,440 per year, or $23.8 per hour.

Research Assistant, Baptist MD Anderson Clinical Trial Office, Baptist Downtown

Baptistjax

Pavilion, NY • On-site

Full-time

Re-posted 28 days ago

Job description

About Baptist Health
Recognized as a top place to work in health care, Baptist Health cares for more patients in Northeast Florida than any other provider, ranking as "most preferred" for more than 30 years. We're Jacksonville's only locally governed, faith-based, not-for-profit health system and provide a full spectrum of preventive and specialty care through 200+ locations and six hospitals. Our centers of excellence include Baptist MD Anderson Cancer Center, Baptist Heart Hospital, Baptist Neurological Institute and Wolfson Children's Hospital.

Baptist Health is hiring a Research Assistant to join the BMDA Clinical Trial Team. This is a full-time, in-person opportunity located on the downtown Jacksonville campus of Baptist MD Anderson.

Participates in conducting literature reviews, collect, and analyze all data related to study including patient recruitment and finance. Manages and responds to project related e-mails, attend project meetings develop minutes, monitor the project budget. Contacts patient follow-up phone calls. Compiles data for progress reports. Performs miscellaneous job-related duties as assigned.

If interested, apply today!

Experience:

  • 1-2 years Clinical Experience Preferred

  • 1-2 years Clinical Research Experience Preferred

  • 1-2 years Experience in an office setting Preferred

Education/Degree Required:

High School Diploma

Degree Preferred:

Associate of Arts/Science

Bachelor of Science in Public Health

Bachelor of Science (non Nursing)

Bachelor of Health Science

Primary Location:

Downtown - Pavilion

Apply