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Irb Jobs in Raleigh, NC (NOW HIRING)

(Clinical) Research Technician

Morrisville, NC

$16.75 - $23.25/hr

Understand and interpret study IRB requirements, SOPs, and protocol-specific instructions to ensure compliant handling of all biospecimens. * Practice and maintain sterile technique throughout all ...

Main duties: • Assisting in communication with the IRB including the preparation of IRB protocols under the supervision of the lab's PI. • Assisting in identifying, recruiting and consenting ...

Assisting in communication with the IRB including the preparation of IRB protocols under the supervision of the lab's PI. Assisting in identifying, recruiting and consenting eligible healthy controls ...

Clinical Research Coordinator

Durham, NC · On-site

$23.50 - $31.25/hr

Communicates with the IRB staff and reviewers and handles issues appropriately. Prepares and submits documents needed for regulatory and safety reporting to sponsors and other agencies. May train or ...

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Irb information

What is the job of the IRB?

An Institutional Review Board (IRB) is a committee that reviews and approves research involving human subjects to ensure ethical standards and participant safety are maintained. IRB members evaluate research protocols, consent processes, and risk management, often requiring knowledge of federal regulations and ethical guidelines. Their work is essential in research institutions to protect participant rights and ensure compliance with regulations.

What are the key skills and qualifications needed to thrive as an IRB (Institutional Review Board) Administrator, and why are they important?

To thrive as an IRB Administrator, you need expertise in research ethics, regulatory compliance, and human subject protection, usually supported by a relevant bachelor's or master's degree. Familiarity with IRB management software, federal regulations (such as the Common Rule), and certifications like CIP (Certified IRB Professional) are typically required. Strong organizational skills, attention to detail, and effective communication are crucial for coordinating reviews and guiding researchers. These skills ensure ethical research practices, regulatory compliance, and the protection of research participants.

What are the typical responsibilities of an IRB coordinator, and how do they interact with researchers and regulatory bodies?

An IRB (Institutional Review Board) coordinator is responsible for managing the review process of research protocols involving human subjects to ensure compliance with ethical standards and federal regulations. This role involves working closely with researchers to guide them through the submission process, reviewing applications for completeness, and facilitating communication between the IRB committee and research teams. Coordinators also serve as liaisons with regulatory bodies, maintain records, and help organize IRB meetings. Strong organizational, communication, and regulatory knowledge are essential, as coordinators often balance multiple projects and deadlines while ensuring research integrity and participant safety.

What is an IRB?

An Institutional Review Board (IRB) is a committee established to review and approve research involving human subjects. The primary purpose of the IRB is to ensure that the rights, welfare, and privacy of participants are protected throughout the research process. IRBs review research proposals to ensure ethical standards are met and that risks to participants are minimized. They are required for most research conducted at universities, hospitals, and other organizations that receive federal funding.

How much do IRB members make?

IRB (Institutional Review Board) members typically do not receive regular salaries; instead, they may be compensated per meeting or receive stipends, often ranging from $50 to $200 per meeting. Compensation varies by institution and the level of involvement, with many members serving voluntarily or as part of their professional duties.

How to get a job on an IRB?

To work with an Institutional Review Board (IRB), candidates typically need a background in research ethics, healthcare, or related fields, along with knowledge of federal regulations such as the Common Rule. Relevant experience, certifications like CITI Program training, and understanding of human subjects research are often required. Positions may include IRB coordinator, administrator, or reviewer, and require strong organizational and communication skills.

What jobs pay 4000 a week without a degree?

Jobs related to IRB (Institutional Review Board) roles typically do not pay $4,000 a week without specialized experience or advanced education. However, high-paying roles in sales, real estate, or skilled trades such as construction or certain tech positions can reach or exceed this level with experience and strong performance. Most high-earning jobs without a degree require specific skills, certifications, or licensing.

What is the difference between Irb vs Clinical Research Coordinator?

AspectIrbClinical Research Coordinator
Required CredentialsOften requires IRB training, ethics certificationRequires research experience, sometimes certifications
Work EnvironmentReview boards, research institutionsClinical sites, hospitals, research centers
Employer & Industry UsageUsed in research oversight, ethics reviewUsed in managing clinical trials, patient coordination
Common Search & Comparison IntentUnderstanding roles in research ethicsUnderstanding clinical trial management

IRBs (Institutional Review Boards) focus on ethical review and approval of research protocols, ensuring participant safety. Clinical Research Coordinators manage the day-to-day operations of clinical trials, including patient recruitment and data collection. While both roles are integral to clinical research, IRBs oversee ethical compliance, whereas Coordinators handle trial execution.

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 cities near Raleigh, NC are hiring for Irb jobs? Cities near Raleigh, NC with the most Irb job openings:

IRB Operations Specialist (Remote)

WIRB-Copernicus Group (WCG)

Cary, NC • On-site, Remote

$19.50/hr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 5 days ago


Job description

General Information
Location: Cary, NC, Remote
Organization: WCG IRB
Job Type: Full Time - Regular
Description and Requirements
ABOUT WCG:
WCG's clinical solutions are built on a foundation of best-in-class clinical services companies. We deliver transformational solutions that stimulate growth, foster compliance, and maximize efficiency for those performing clinical trials. WCG is proud to serve individuals on the frontlines of science and medicine, and the organizations striving to develop new products and therapies to improve the quality of human health. It is our role to empower them to accelerate advancement, while ensuring the risks of progress never outweigh the value of human life.
WHY WE LOVE WCG:
At WCG, our employees are our most valuable asset and as with all our assets, we invest in them with an eye toward future success. We provide each eligible employee with a comprehensive set of benefits designed to protect their personal and financial health and to help them make the most of their future.
  • Comprehensive Benefits package - Health, Dental, Vision, Life Disability, 401k with match, and flexible spending accounts
  • Employee Assistance Programs and additional work/life resources
  • Referral Bonuses and Tuition Reimbursement
  • Accrued PTO
  • Volunteer Time Off to benefit the community
  • Opportunities for career development with on-the-job training, certification assistance, and continuing education reimbursement

The hourly rate for this position is $19.50 - $ 28.10. This rate may vary based on the candidate's qualifications, experience, skills, education, and geographic location.
JOB SUMMARY:
Responsibilities include, but are not limited to supporting data collection, the management
and analysis of documents, client reporting and problem resolution. This position will:
  • Support the Board and clients by preparing documents for review in accordance with company policies and regulatory requirements
  • Provide accurate document identification and data entry
  • Finalize and deliver documents to clients
  • Meet assigned metrics around speed and accuracy
  • Able to deal effectively with high work volume, rigid deadlines, and frequent changes

Specific job function requirements are outlined on training curriculum and addenda that supports step level 1 development in this position. Each function is made up of multiple duties. Specific criteria have been attributed to each duty to measure proficiency. As proficiency is proven in each duty, additional duties will be assigned for learning.
ESSENTIAL DUTIES/RESPONSIBILITIES:
To perform this job successfully, an individual must be able to perform each essential duty and responsibility satisfactorily. The accountabilities listed below are representative of the knowledge, skills, and/or ability required.
  • Ability to maintain and promote positive working relationships with clients (internal and external) by providing timely and professional service to their needs within the scope of company mission and accompanying regulations
  • Maintain close attention to detail
  • Ability to proof-read and detect errors in typing, spelling, grammar, syntax, and punctuation
  • Ability to read and interpret documents such as protocols for clinical investigations, medical, literature, safety rules, operating and maintenance instructions
  • Ability to set priorities and manage time effectively
  • Accurately and completely enter information in a database system
  • Contribute to a positive team environment through collaborative engagement with others
  • Resolve questions and problems effectively
  • Communicate to obtain information or clarify requests
  • Mentor team members by teaching procedures, monitoring, and proofing work, and providing constructive feedback as needed or requested
  • Is able to assist others across Operations, as needed. This may include overtime requests, training support, etc.
  • Professional/oral written communication skills
  • Independent worker
  • Accountable for self-metrics
  • Other duties as assigned by supervisor. These may, on occasion, be unrelated to the position described here.
  • Attendance and punctuality are essential functions of the position.
  • Other duties as assigned by supervisor. These may, on occasion, be unrelated to the position described here.

EDUCATION REQUIREMENTS:
  • Bachelors or Associates Degree preferred, or a combination of equivalent education and experience

QUALIFICATIONS/EXPERIENCE:
  • Two+ years of experience working in an office setting where proofing documents and attention to detail are essential elements of your job requirements
  • Must have strong analytical skills with a high degree of accuracy in work
  • Advanced knowledge of Microsoft Word, Excel, Outlook, Databases and Adobe
  • Knowledge of FDA regulations as they relate to research (preferred)
  • Must be able to maintain confidentiality
  • Experience working with medical terminology (preferred)
  • Ability to work independently, utilize discretionary judgment, and be a pro-active team player
  • Exhibit excellence in:
    • Communication - Proficient verbal and written communication skills. Willingness to share and receive information and ideas from all levels of the organization in order to achieve the desired results.
    • Customer service- understanding the importance of meeting client requests and adapting to changing needs
    • Teamwork - Commitment to the successful achievement of team and organizational goals through a desire to participate with and help other members of the team

TRAVEL REQUIREMENTS: 0% - 5%
Physical and Sensory Requirements:
The physical and sensory requirements described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be offered to individuals with disabilities to assist in performing the essential functions of the position. Work activities involve light to moderate physical effort (for example, sitting in one place for extended periods of time, standing, walking, bending, lifting lightweight objects, intermittent to sustained periods of keyboarding). Majority of time is spent in a seated position with frequent opportunity to move about at will. Activities require a variety of easy muscle movements. Work activities involve a frequent need to concentrate on a variety of sensory inputs for moderate to lengthy durations at a time requiring diligence and attention to interpret effectively. There will be a need to attend to single or simultaneous tasks where accuracy of details is important. The need for detailed and precise work is high.
US Specific Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Position Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms.
WCG is proud to be an equal opportunity employer - Qualified applicants will receive consideration for employment based on merit and without regard to race, color, national origin or ancestry, religion or creed, sex, sexual orientation, gender expression, gender identity, age, marital status, family or parental status, disability, genetic information, citizenship, veteran status, or any other legally recognized basis or status protected by federal, state, or local law. WCG complies with the Vietnam Era Veterans' Readjustment Act and Section 503 of the Rehabilitation Act. We promote a "One WCG" culture where all are welcome, respected, valued, and empowered to make a difference every day to advance clinical research.