ZipRecruiter

Log In

1

Irb Coordinator Jobs in Raleigh, NC (NOW HIRING)

UNC-Chapel Hill

Clinical Research Assistant

Chapel Hill, NC · On-site

$19 - $21/hr

... include coordinating and processing the administrative and regulatory paperwork associated with ... This position may assist in preparation of documents required for IRB initial and continuing review ...

Science 37

Site Operations Specialist

Morrisville, NC · On-site

$50 - $70/hr

... IRB, central lab) a plus * Proficient in Microsoft Office and Google Applications * Experience with dashboards or reporting tools is a plus * Scheduling and Logistics Coordination * Experience ...

Science 37

Site Operations Specialist

Morrisville, NC · On-site

... IRB, central lab) a plus * Proficient in Microsoft Office and Google Applications * Experience with dashboards or reporting tools is a plus * Scheduling and Logistics Coordination * Experience ...

Science 37

Site Operations Specialist

Morrisville, NC · On-site

... IRB, central lab) a plus * Proficient in Microsoft Office and Google Applications * Experience with dashboards or reporting tools is a plus * Scheduling and Logistics Coordination * Experience ...

company274

Clinical Research Assistant

Raleigh, NC · On-site

... IRB)-approved study protocol and/or manual of procedures. Day-to-day activities may include all or ... Observe Coordinator in patient care and management. * Assist Coordinator in monitoring subject flow ...

Veranex

Sr Clinical Research Associate

Raleigh, NC · On-site

$98K - $140K/yr

... IRB)/Ethics Committee (EC) requirements during clinical studies by training/guidance of investigators/research coordinators, conducting periodic on-site evaluations and follow-up of corrective ...

Fortrea

FSP Study Start-Up Associate

Durham, NC · On-site

... EC/IRB/Third body/Regulatory Authority submissions are made within the timelines agreed with ... This includes effective communication and coordination with key business stakeholders (e.g., study ...

UNC HEALTH

Director Clinical Research

Raleigh, NC · On-site

Ensures IRB policies and procedures are followed. Provides operational and administrative leadership, including oversight of the clinical team and regulatory specialist. Coordinates with ancillary ...

New

previous pagenext page

Showing results 21-40

All JobsIrb JobsIrb Coordinator JobsIrb Coordinator Jobs in Raleigh, NC

Irb Coordinator information

See Raleigh, NC salary details

$26.2K

$56.3K

$98.7K

How much do irb coordinator jobs pay per year?

As of Sep 2, 2026, the average yearly pay for irb coordinator in Raleigh, NC is $56,250.00, according to ZipRecruiter salary data. Most workers in this role earn between $39,400.00 and $67,600.00 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 Raleigh, NC?

The most popular types of Irb jobs in Raleigh, NC are:

What are popular job titles related to Irb Coordinator jobs in Raleigh, NC?

For Irb Coordinator jobs in Raleigh, NC, the most frequently searched job titles are:

What job categories do people searching Irb Coordinator jobs in Raleigh, NC look for?

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

What cities near Raleigh, NC are hiring for Irb Coordinator jobs?

Cities near Raleigh, NC with the most Irb Coordinator job openings:

Irb Coordinator jobs near you
Infographic showing various Irb Coordinator job openings in Raleigh, NC as of August 2026, with employment types broken down into 1% As Needed, 85% Full Time, 11% Part Time, 1% Temporary, and 2% Contract. Highlights an 78% Physical, 2% Hybrid, and 20% Remote job distribution, with an average salary of $56,250 per year, or $27 per hour.

Senior Clinical Research Coordinator

Velocity Clinical Research, Inc.

Raleigh, NC • On-site

$21.50 - $28.50/hr

Part-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 7 days ago

Velocity Clinical Research rating

7.3

Company rating: 7.3 out of 10

Based on 5 frontline employees who took The Breakroom Quiz

74th of 120 rated laboratories

Job description

Overview
Velocity Clinical Research is an owned and integrated research site organization, providing excellence in patient care, high quality data and fully integrated research sites. At Velocity, we align our values and behaviors to give our employees the best chance of delivering on our brand promise: to bring innovative medical treatments to patients. We are committed to making clinical trials succeed by generating high quality data from as many patients as possible, as quickly as possible while providing exemplary patient care at every step.
As an employee of Velocity, you are the most integral part of our mission. For talented candidates who perform at a high level, Velocity will invest to support career advancement and reward performance. Whether you are new to clinical research or are an industry veteran, we invite you to apply to Velocity.
Benefits include medical, dental and vision insurance, paid time off and company holidays, 401(k) retirement plan with company-match, and an annual incentive program.
Summary:
Subject matter expert and leader of a clinical trial team to conduct and manage clinical trial(s) from start up through study close out in accordance with the study protocol, GCP, and Velocity's SOPs.
Responsibilities
Duties/Responsibilities:
  • Serve as leader of a study team to execute clinical trials
  • Mentor and train staff in the conduct of clinical trials, protocol requirements, communication,
    and trial management skills
  • Create training strategies and mitigation plans
  • Conduct and manage clinical trials in accordance with the study protocol, GCP, ICH Guidelines
    and Velocity's SOPs
  • Implement and coordinate assigned clinical trials including start up, vendor management,
    subject recruitment, source development review, scheduling subjects, protocol training,
    collection of regulatory documents, conducting visits, ensuring data is entered in a timely
    manner and all queries are resolved, managing and reporting adverse events, serious adverse
    events, and deviations, implementing new protocol amendments, providing all close out
    reports.
  • Apply project management concepts to manage risk and improve quality in the conduct of a
    clinical research study
  • Develop, coordinate, and implement research and administrative strategies to successfully
    manage assigned protocols.
  • Communicate effectively and professionally with coworkers, leadership, study subjects,
    sponsors, CROs, and vendors.
  • Ensure good documentation practices are applied by team members when collecting and
    correcting data, transferring data to sponsor/CRO data capture systems and resolving queries
  • Ensure confidentiality of patient protected health information, sponsor confidential information
    and Velocity confidential information is maintained by all team members
  • Develop communication and escalation strategies within teams to that ensure patient safety is
    upheld and all adverse events, serious adverse events, and adverse events of special interest
    are followed and reported in accordance with the protocol and Velocity SOPs
  • Ensure all data is entered into the sponsor's data portal and all queries are resolved in a timely
    manner
  • Ensure staff are delegated and trained appropriately and documented
  • Ensure the creation, collection and submission of regulatory documents to Sponsors and IRBs
    as required per protocol, GCP/ICH regulations and IRB requirements.
  • Evaluate potential subjects for participation in clinical trials including phone and in person pre screens.
  • Create and execute recruitment strategies in conjunction with patient recruitment staff
  • Incorporate key timelines, endpoints, required vendors, and patient population when planning
    for each assigned protocol.
  • Incorporate understanding of how decisions affect the bottom-line including links between
    operations and company's financial performance and how it is essential to create value of all
    stakeholders of the organization when planning for each assigned protocol.
  • Incorporate understanding of product development lifecycle and significance of protocol
    design including critical data points when planning for each assigned protocol
  • Develop Quality Control strategies for team member projects
  • Perform clinical duties (e.g. Drug preparation and administration, fibroscan, phlebotomy, ECG,
    lab processing) within scope
  • Promote respect for cultural diversity and conventions with all individuals.
  • Understand the disease process or condition under study
  • Other duties as assigned

Qualifications
Education/Experience:
  • Bachelor's degree and 4 years as a Clinical Research Coordinator OR
  • Associate's degree and 6 years as a Clinical Research Coordinator OR
  • High School Graduate and/or technical degree and 8 years as a Clinical Research Coordinator

Required Licenses/Certifications:
  • Phlebotomy if applicable and required by state law
    Intravenous/Intramuscular dose administration and preparation if applicable and required by state law
    Certified Clinical Research Coordinator through ACRP or SOCRA within six months of being in the role

Required Skills:
  • Advanced knowledge of medical terminology
  • Proficient in the use of the following technology: Computers, Microsoft Office software, fax, copier, and multi-line telephone.
  • Profcient ability to work in a fast-paced environment
  • Advanced verbal, written, and organizational skills
  • Advanced interpersonal and communication skills
  • Advanced ability to work as a team player
  • Advanced ability to read, write, and speak English
  • Demonstrated ability to multi-task
  • Advanced ability to follow written guidelines
  • Demonstrated ability to work independently, plan and prioritize multiple deliverables and objectives
  • Demonstrated ability to be flexible/adapt as daily schedule may change rapidly
  • Must be detail oriented
  • Proficient problem solving and strategic decision making ability.
  • Advanced in accepting individual responsibility for actions taken and demonstrating professionalism when judged, critiqued and/or praised.
  • Proficient leader, mentor and team builder

Required Physical Abilites:
  • Sit or stand for long periods of time
  • Travel locally and nationally
  • Communicate in person and by a telephone
  • Limited walking required
  • Limited to lifting up to 30 pounds

NOTE: The above Job Description is intended to communicate the general function of the mentioned position and by no means should be considered an exhaustive or complete outline of the specific tasks and functions that will be required. Additionally, specific tasks and duties of the position are subject to change as the Company, the department and circumstances change. All employees are expected to perform their duties within their ability as required by the job and/or as requested by management.

What Velocity Clinical Research employees say

Hours and flexibility

Workplace

Get the full story on Breakroom

Apply