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

System One

Clinical Research Coordinator

Rochester, NY · On-site

$26 - $30/hr

Coordinate and schedule study visits, procedures, and follow-up activities with study participants and clinical teams. * Collect, record, and maintain accurate clinical research data and source ...

System One

Clinical Research Coordinator

Rochester, NY · On-site

$26 - $30/hr

Coordinate and schedule study visits, procedures, and follow-up activities with study participants and clinical teams. * Collect, record, and maintain accurate clinical research data and source ...

System One

Clinical Research Nurse

Rochester, NY · On-site

$40 - $50/hr

Clinical Research Nurse Location: Rochester, NY Type: Contract To Hire Compensation: $40.00 - $50 ... Manage all aspects of a study ensuring adherence to the protocol, GCP, and applicable regulations ...

System One

Clinical Research Nurse

Rochester, NY · On-site

$40 - $50/hr

Clinical Research Nurse Location: Rochester, NY Type: Contract To Hire Compensation: $40.00 - $50 ... Manage all aspects of a study ensuring adherence to the protocol, GCP, and applicable regulations ...

System One

Clinical Research Nurse

Rochester, NY · On-site

$40 - $50/hr

Clinical Research Nurse Location: Rochester, NY Type: Contract To Hire Compensation: $40.00 - $50 ... Manage all aspects of a study ensuring adherence to the protocol, GCP, and applicable regulations ...

System One

Clinical Research Nurse

Rochester, NY · On-site

$40 - $50/hr

Manage all aspects of a study ensuring adherence to the protocol, GCP, and applicable regulations, including participating in the informed consent process, coordinating, and performing all study ...

System One

Clinical Research Nurse

Rochester, NY · On-site

$40 - $50/hr

Manage all aspects of a study ensuring adherence to the protocol, GCP, and applicable regulations, including participating in the informed consent process, coordinating, and performing all study ...

System One

Clinical Research Nurse

Rochester, NY · On-site

$40 - $50/hr

Manage all aspects of a study ensuring adherence to the protocol, GCP, and applicable regulations, including participating in the informed consent process, coordinating, and performing all study ...

System One

Clinical Research Nurse

Rochester, NY · On-site

$40 - $50/hr

Manage all aspects of a study ensuring adherence to the protocol, GCP, and applicable regulations, including participating in the informed consent process, coordinating, and performing all study ...

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All JobsClinical Research Study JobsClinical Research Study Jobs in Rochester, NY

Clinical Research Study information

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How much do clinical research study jobs pay per hour?

As of Aug 5, 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 July 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.

Clinical Research Coordinator

ALLIANCE CLINICAL LLC

Rochester, NY • On-site

$28 - $30/hr

Temporary

Posted 8 days ago

Job description

*This is a full-time, temporary position currently estimated to last until December 31, 2026 (subject to business needs). There may be the possibility for this position to become permanent.*


Summary:

The Clinical Research Coordinator (CRC) supports the coordination and execution of clinical research studies within a healthcare setting. This role ensures clinical trials are conducted in compliance with study protocols, regulatory requirements, and institutional policies while protecting participant safety and data integrity. Working closely with Principal Investigators (PIs), research staff, and study participants, the CRC assists with participant screening, data collection, and the coordination of study activities to ensure accuracy, efficiency, and high-quality research outcomes.


Essential Duties and Responsibilities:

  • Assist in the coordination and execution of clinical research protocols under the supervision of the PI and senior research staff
  • Conduct screening visits to collect medical history & other information from study participants
  • Assist with informed consent and enrollment of study participants in accordance with protocol requirements and ethical guidelines
  • Coordinate and schedule study visits, procedures, and follow-up activities with study participants and clinical teams
  • Collect, record, and maintain accurate clinical research data and source documentation in compliance with regulatory and institutional standards
  • Communicate with study participants to provide education, answer questions, and support adherence to study requirements
  • Monitor study progress and report adverse events, protocol deviations, and other study-related issues to the research team
  • Adhere to site standard operating procedures (SOPs) and Good Clinical Practice (GCP) guidelines
  • Draw, process, and ship laboratory specimens, including the handling of dangerous goods, in accordance with regulations (if qualified)
  • Scan, upload, file, and maintain organized study records and documentation
  • Apply critical thinking skills to support efficient study operations and problem resolution
  • Perform other duties as assigned

Qualifications:

  • High school diploma or equivalent required; an associate’s degree or higher in a health-related field preferred
  • Basic knowledge of clinical research strongly preferred
  • Medical terminology & patient care experience required
  • Strong organizational, time management, and attention-to-detail skills with the ability to manage multiple priorities
  • Ability to communicate clearly and professionally with diverse populations
  • Ability to work collaboratively in a fast-paced, team-oriented environment
  • Knowledge of GCP, HIPAA, ALCOA principles, FDA regulations, and IATA guidelines strongly preferred
  • Experience with participant screening and the informed consent process strongly preferred
  • Proficiency with electronic data capture systems, clinical trial management software, and Microsoft Office (Excel, Word, and PowerPoint) preferred


Certificates, Licenses, and Registrations:

  • Medical Assistant (MA) certification preferred
  • Current CPR/BLS certification preferred
  • Certification as a Clinical Research Coordinator (e.g., CCRC) or a willingness to obtain certification preferred


ACN does not provide visa sponsorship for this role. Candidates who will require immigration or visa sponsorship at any time now or in the future (including, but not limited to, H‑1B, TN, or STEM OPT training plans) are not eligible for this role.


About the Company:

At Alliance Clinical Network, our mission is to advance medical research by enrolling diverse populations in high-quality clinical trials. We are committed to maintaining the highest standards of integrity and excellence, and to ensuring that every participant receives respectful and compassionate care. We strive to build a tightly knit, supportive and collaborative environment where our team members can thrive and make meaningful contributions to human health.