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Irb Coordinator Jobs in Rochester, NY (NOW HIRING)

System One

Clinical Research Nurse

Rochester, NY · On-site

$40 - $50/hr

... process, coordinating, and performing all study visit procedures per protocol, managing ... Ensure Serious Adverse Events (SAE's) are reported to Principal Investigator, Sponsor, and IRB ...

System One

Clinical Research Nurse

Rochester, NY · On-site

$40 - $50/hr

... process, coordinating, and performing all study visit procedures per protocol, managing ... Ensure Serious Adverse Events (SAE's) are reported to Principal Investigator, Sponsor, and IRB ...

System One

Clinical Research Nurse

Rochester, NY · On-site

$40 - $50/hr

... process, coordinating, and performing all study visit procedures per protocol, managing ... Ensure Serious Adverse Events (SAE's) are reported to Principal Investigator, Sponsor, and IRB ...

System One

Clinical Research Nurse

Rochester, NY · On-site

$40 - $50/hr

... process, coordinating, and performing all study visit procedures per protocol, managing ... Ensure Serious Adverse Events (SAE's) are reported to Principal Investigator, Sponsor, and IRB ...

System One

Clinical Research Nurse

Rochester, NY · On-site

$40 - $50/hr

... process, coordinating, and performing all study visit procedures per protocol, managing ... Ensure Serious Adverse Events (SAE's) are reported to Principal Investigator, Sponsor, and IRB ...

System One

Clinical Research Nurse

Rochester, NY · On-site

$40 - $50/hr

... process, coordinating, and performing all study visit procedures per protocol, managing ... Ensure Serious Adverse Events (SAE's) are reported to Principal Investigator, Sponsor, and IRB ...

System One

Clinical Research Nurse

Rochester, NY · On-site

$40 - $50/hr

... process, coordinating, and performing all study visit procedures per protocol, managing ... Ensure Serious Adverse Events (SAE's) are reported to Principal Investigator, Sponsor, and IRB ...

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Irb Coordinator information

See Rochester, NY salary details

$26.7K

$57.1K

$100.2K

How much do irb coordinator jobs pay per year?

As of Sep 1, 2026, the average yearly pay for irb coordinator in Rochester, NY is $57,123.00, according to ZipRecruiter salary data. Most workers in this role earn between $40,000.00 and $68,600.00 per year, depending on experience, location, and employer.

What is an IRB coordinator?

IRB Coordinators are professionals who manage and oversee the processes of Institutional Review Boards (IRBs), which are committees responsible for reviewing and approving research involving human subjects. Their main duties include ensuring compliance with federal regulations, guiding researchers through the IRB submission process, and maintaining documentation for approved studies. IRB Coordinators act as a liaison between researchers, board members, and regulatory agencies to protect the rights and welfare of research participants. They play a critical role in maintaining ethical standards in research institutions.

What are the key skills and qualifications needed to thrive as an IRB coordinator?

To thrive as an IRB Coordinator, you need a thorough understanding of research ethics, federal regulations, and human subjects protection, typically supported by a bachelor's degree in a relevant field. Familiarity with IRB management systems, compliance tracking tools, and often CITI Program certification is essential. Strong attention to detail, organizational skills, and effective communication are critical soft skills for managing submissions and liaising with researchers. These competencies ensure ethical research practices, regulatory compliance, and smooth IRB operations.

What are some common challenges faced by IRB coordinators when managing multiple research protocols simultaneously?

IRB Coordinators often juggle several research protocols at once, which requires strong organizational and time management skills. Common challenges include ensuring timely reviews, tracking protocol amendments, and maintaining compliance with evolving regulations. Coordinators must communicate effectively with investigators to resolve documentation issues and clarify ethical concerns. Balancing these tasks while adhering to strict deadlines can be demanding, but it also offers opportunities to develop expertise in research ethics and regulatory affairs.

How much does an IRB coordinator make?

An IRB coordinator typically earns between $50,000 and $80,000 annually, depending on experience, education, and location. They often require knowledge of federal regulations and institutional review board processes, with some positions offering additional benefits or certifications.

How to become an IRB coordinator?

To become an IRB coordinator, candidates typically need a bachelor's degree in health sciences, research, or a related field, along with experience in research compliance or ethics. Certification from organizations like the Certified IRB Professional (CIP) can enhance job prospects. Strong organizational skills and knowledge of federal regulations governing human subjects research are essential for this role.

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

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

What are popular job titles related to Irb Coordinator jobs in Rochester, NY?

For Irb Coordinator jobs in Rochester, NY, the most frequently searched job titles are:

What job categories do people searching Irb Coordinator jobs in Rochester, NY look for?

The top searched job categories for Irb Coordinator jobs in Rochester, NY are:

What cities near Rochester, NY are hiring for Irb Coordinator jobs?

Cities near Rochester, NY with the most Irb Coordinator job openings:

Irb Coordinator jobs near you
Infographic showing various Irb Coordinator job openings in Rochester, NY as of August 2026, with employment types broken down into 1% As Needed, 85% Full Time, 11% Part Time, 1% Temporary, 1% Contract, and 1% Nights. Highlights an 81% Physical, 2% Hybrid, and 17% Remote job distribution, with an average salary of $57,123 per year, or $27.5 per hour.

Human Subjects Research Coordinator II

University of Rochester

Rochester, NY • On-site

$25.14 - $35.24/hr

Full-time

Re-posted 24 days ago

University Of Rochester rating

8.3

Company rating: 8.3 out of 10

Based on 188 frontline employees who took The Breakroom Quiz

127th of 627 rated colleges and universities

Job description

As 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):
220 Hutchison Rd, Rochester, New York, United States of America, 14620
Opening:
Worker Subtype:
Regular
Time Type:
Full time
Scheduled Weekly Hours:
40
Department:
400094 Neurology - NMD M & D
Work Shift:
UR - Day (United States of America)
Range:
UR URG 108 H
Compensation Range:
$25.14 - $35.24
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:
The Neuromuscular Disease Study Coordinator II will manage projects primarily in Facioscapulohumeral Muscular Dystrophy, with the ability to work on projects in other neuromuscular diseases. The research projects in the group include observational studies, clinical trials, and multi-center clinical research studies in both adult and pediatric subjects. The Study Coordinator II will have considerable latitude for independent judgment and will coordinate all aspects of assigned human subject research studies. This role provides assistance to the Principal Investigator(s) and works as an integral part of the research team. This role mentors Human Subject Research Coordinator I(s) and supervises students as assigned.
ESSENTIAL FUNCTIONS
  • Uses independent clinical judgment to recruit, consent, enroll and retain study subjects across the NMD portfolio of human subjects' studies. Develops, implements, and evaluates subject recruitment and retention strategies. Creates and modifies patient recruitment material as necessary. Manages and updates registries used for subject recruitment.
  • Coordinates, schedules, and conducts research study visits according to the protocol to support successful achievement of milestones, specific aims, and study objectives. Performs study-related procedures as outlined in the protocol. Training will be provided to implement protocol's procedures. Coordinates and documents dispensing and returning of study drugs/materials, as applicable. Resolves study subject questions and concerns, triaging to Principal Investigator, as necessary. Ensures patient clinical care resources are available to support conduct of human subject studies in accordance with protocol. Inputs/regularly updates and reviews all patient information in the patient databases to ensure the most accurate databases possible, including resolving data queries timely.
  • Mentors and trains NMD Study Coordinators (HSRC I) on activities related to conducting human subject research and provides back-up support across the team as needed. Directs, understands, implements, and provides training on most recent study protocol (e.g., amended protocol), procedures, documentation, and use of study materials to subjects and team members as appropriate. Ensures compliance, following up and communicating as needed. Keeps current with study-specific training, including understanding specific details of study protocol, all relevant sponsor and institutional policies, standard operating procedures, and guidelines. Troubleshoots and resolves operational issues related to studies.
  • Develops, modifies and maintains regulatory requirements for multiple research studies. Manages IRB submissions to include study applications, amendments and continuing reviews. Creates, modifies, organizes, and maintains study documentation for the regulatory file. Ensures consistency and standardization of protocol activities across multiple sites. Responsible for monitoring compliance with all regulatory and institutional policies, and takes corrective action on issues identified. Trains on federal, state, sponsor, and/or institutional regulations, policies, and practices related to human subject research.
  • Serves as the liaison between cross-functional research team, additional research sites, research administration, study sponsors, and IRB to facilitate communication, resolves issues, and enhance collaboration. Works with research administration team on pre-award and study start up documents providing expertise related to time studies and budget feasibility for study procedures, overall complexity and effort required for completing studies. Reviews study progress, including communicating with research administrator and updating OnCore or other workbooks on enrollment, visits, and other study procedures completed to ensure maximum payment is received and expenses are monitored in accordance with budget. Represents the University and Principal Investigator at study meetings, as needed. Schedules, prepares for, and attends study sponsor monitor meetings in accordance with protocol.
  • Develops and/or manages databases for research studies. Ensures data is entered in a timely manner and database(s) is up-to-date. Exports research data or work with Data Office staff to obtain data for analysis and preparation of presentations, abstracts, and publications. Develops, implements, and monitors systems and methods to ensure data integrity. Assist in chart abstraction for the maintenance of patient databases.
  • Demonstrates accountability for continuous learning related to clinical research. Attends training sessions and other educational opportunities related to clinical research in order to keep current with Good Clinical Practice guidelines, federal and state polices and laws, institutional certifications, industry standards and best practices, and trends in relevant therapeutic areas. Participates in study team meetings and provides updates on project status and changes in regulatory requirements as needed.
  • Other duties as assigned

MINIMUM EDUCATION & EXPERIENCE
  • Bachelor's degree and 2 years of experience in human subject research coordination required
  • Or equivalent combination of education and experience
  • If applicable, department specific experience required
  • Experience as a Phlebotomist preferred

KNOWLEDGE, SKILLS AND ABILITIES
  • Word processing and data analysis software required
  • Experience as Human Subject Research Coordinator I preferred
  • Experience with Excel spreadsheets and electronic databases preferred

LICENSES AND CERTIFICATIONS
  • SOCRA - Certification In Clinical Research upon hire preferred
  • Association of Clinical Research Professionals (ACRP) upon hire preferred

The 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.

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