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Irb Consultant Jobs in Raleigh, NC (NOW HIRING)

Veranex

Sr Clinical Research Associate

Raleigh, NC · On-site

$98K - $140K/yr

... and reimbursement consulting. The Veranex Clinical Operations team is a dynamic group of ... IRB)/Ethics Committee (EC) requirements during clinical studies by training/guidance of ...

Duke Health

PHYSICIAN ASSISTANT Hospital Medicine

Durham, NC · On-site

$96K - $130K/yr

The PA contributes to excellence in patient care, research, teaching, consulting, and provides ... Support IRB approved clinical research/trials though a variety of activities including but not ...

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How much do irb consultant jobs pay per hour?

As of Aug 22, 2026, the average hourly pay for irb consultant in Raleigh, NC is $40.39, according to ZipRecruiter salary data. Most workers in this role earn between $28.51 and $48.12 per hour, depending on experience, location, and employer.

What is an IRB consultant?

IRB Consultants are professionals who provide expertise and guidance on Institutional Review Board (IRB) processes and compliance. They assist organizations, researchers, and institutions in ensuring that human subjects research meets ethical standards and regulatory requirements. Their services may include protocol review, training, IRB submission support, policy development, and navigating federal regulations. IRB Consultants help streamline the review process and minimize risks associated with research involving human participants.

What skills and qualifications are needed to be an IRB consultant?

To thrive as an IRB Consultant, you need a solid understanding of research ethics, federal regulations (such as 45 CFR 46), and experience in human subjects protection, often supported by a relevant degree and prior IRB or research compliance experience. Familiarity with IRB management software, CITI certification, and knowledge of compliance tracking systems are typically required. Strong analytical skills, attention to detail, and effective communication are crucial soft skills for advising researchers and ensuring ethical standards. These competencies are vital to safeguard research participants and maintain institutional and regulatory compliance in research activities.

What challenges do IRB consultants face when working with research teams across different institutions?

IRB Consultants often encounter challenges such as navigating varying institutional policies, managing diverse expectations, and ensuring compliance with differing federal, state, and local regulations. Collaborating with researchers who have varying levels of experience with IRB processes can require clear communication and tailored guidance. Building consensus among stakeholders, especially when protocols involve multiple sites, is also a key part of the role, requiring strong organizational and interpersonal skills.

What is the difference between Irb Consultant vs Clinical Research Coordinator?

AspectIrb ConsultantClinical Research Coordinator
CredentialsTypically requires IRB-related certifications, research compliance trainingRequires research experience, often with certifications like CCRC or CCRP
Work EnvironmentAdvises on IRB submissions, compliance, and protocol reviewManages daily clinical trial activities, patient interactions
Employer & IndustryResearch institutions, hospitals, biotech firmsHospitals, research centers, pharmaceutical companies

While both roles are involved in clinical research, an Irb Consultant primarily focuses on IRB submissions, compliance, and ethical review processes. In contrast, a Clinical Research Coordinator manages the day-to-day operations of clinical trials, including patient recruitment and data collection. Both roles require knowledge of research protocols and regulations but differ in their specific responsibilities and work focus.

How to become an IRB consultant?

To become an IRB consultant, individuals typically need a background in research, ethics, or healthcare, along with experience in regulatory compliance. Gaining knowledge of federal regulations such as the Common Rule and Good Clinical Practice (GCP) is essential, and certifications like the Certified IRB Professional (CIP) can enhance credibility. Strong analytical skills and attention to detail are important for advising institutions on ethical review processes.

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The top searched job categories for Irb Consultant jobs in Raleigh, NC are:

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Irb Consultant jobs near you
Infographic showing various Irb Consultant job openings in Raleigh, NC as of August 2026, with employment types broken down into 80% Full Time, and 20% Contract. Highlights an 60% In-person, and 40% Remote job distribution, with an average salary of $84,017 per year, or $40.4 per hour.

Clinical Research Study Coordinator

Procom Services

Chapel Hill, NC

$20.75 - $27.50/hr

Contractor

Re-posted 17 days ago

Job description

Company Description

Procom is a leading provider of professional IT services and staffing to businesses and governments in Canada as well as the US.
With revenues over $500 million, the Branham Group has recognized Procom as the 3rd largest professional services firm in Canada and is now the largest "Canadian-Owned" IT staffing/consulting company.
Specialties Contract Staffing (Staff Augmentation)
Permanent Placement (Staff Augmentation)
ICAP (Contractor Payroll)
Flextrack (Vendor Management System)

Job Description

Clinical Research Study Coordinator

On behalf of our client, Procom Services is searching for a Clinical Research Study Coordinator to join their team in Chapel Hill, NC. The primary purpose of this position will be to run all aspects of the assigned clinical trials. IRB submissions, recruitment, working with investigators as well as the patients.


Clinical Research Study Coordinator Job Description

Perform independent and dependable work in preparation and coordination of study submission to IRB and other appropriate committees following regular deadlines.

They will provide draft IRB, Sponsor and other response to the PI for approval.

They will respond on behalf of the PI when appropriate

Communicate with study staff, IRB, sponsors, domestic and international study partners in a courteous and professional manner; Meet with study sponsor representatives as needed.

Attend IRB, study sponsor, or any other meeting in place of the PI

Prepare informed consent forms that follow appropriate regulation and meet sponsor requirements

Address queries and memos from IRB and other committees create draft response to query's for PI approval

Maintain and organize electronic and paper regulatory documents, study files and patient binders.

Perform Quality Assurance/Quality Control of Study files

Track and enter regulatory submissions using electronic databases and prepare reports within the databases.  

Respond to all queries and adverse events in a timely manner.

Will be initial contact for all adverse events for their studies

See clinical trial patients, follow up with phone calls and make sure all protocols are followed. Will also be responsible for screening and recruitment of clinical trial patients

Communicate for themselves and on behalf of the PI potential issues to regulatory supervisor, study team members, and investigators

Assist other staff members in completion of work in a team oriented fashion

Complete other regulatory duties as assigned.

Communication, Teamwork and Compliance

Employee uses effective verbal and written communication to accomplish tasks

Coordinator must have the technical ability to apply the knowledge of research principles when collecting, editing, analyzing the data and reporting data/information related to the study. 

The Coordinator will be required to have general computer and technical knowledge as well as an understanding of patient input data bases. 

Requires ability to identify discrepancies in database information.

Coordinator must be able to problem solve and implant new systems to help make Center more effective. This type of work requires extreme organization and attention to detail.

Coordinator will support research, develop programs and policies for the Center.

Coordinator must be able to work as a productive member of a team by helping develop solutions to meet group needs as well as the structure of the team. 

Coordinator will have the ability to serve as a team leader.

Skills include working effectively with patients, medical faculty and staff, ability to understand and implement protocols and teach them to clinic personnel. 

Requires ability to develop a flexible work schedule, organized and able to implement clinic clinical trials based on FDA and good clinical practice guidelines and work independently.

Experience in research is required. 

Knowledge of research principles and methods to interpret, and coordinate the collection and analysis of data/information related to the research.

Clinical Research Study Coordinator Mandatory Requirements

Prior experience in Clinical Trials.

Nursing degree preferred, specifically with a focus in Oncology.


Clinical Research Study Coordinator Start Date

ASAP


Clinical Research Study Coordinator Assignment Length

6 months (possible extension/hire)

Additional Information
PLEASE NOTE THAT WE ARE NOT ABLE TO WORK WITH CANDIDATES ON H1B VISAS OR CANDIDATES REPRESENTED BY THIRD PARTIES.

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