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Full Time Irb Jobs (NOW HIRING)

Good Samaritan Hospital at 375 Dixmyth Avenue Work Schedule: * Full-Time (80 hours bi-weekly) * Day ... Comply with all IRB/FDA requirements in study submissions. * Assures compliance with IRB/FDA ...

Clinical Research Coordinator

Cincinnati, OH · On-site

$23.25 - $31/hr

... such as IRB/FDA processes, research administration, and sponsor collaboration. Location: Good Samaritan Hospital 375 Dixmyth Ave, Cincinnati, OH 45220 Schedule: Full time, day shift Incentives ...

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Full Time Irb information

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$62K

$330.1K

$400K

How much do full time irb jobs pay per year?

As of Jun 12, 2026, the average yearly pay for full time irb in the United States is $330,066.00, according to ZipRecruiter salary data. Most workers in this role earn between $311,000.00 and $385,500.00 per year, depending on experience, location, and employer.

What is the difference between Full Time Irb vs Part Time Irb?

AspectFull Time IrbPart Time Irb
CredentialsIRB certification, research ethics trainingIRB certification, research ethics training
Work EnvironmentOffice, research institutions, hospitalsFlexible, part-time settings, remote options
Employer & IndustryResearch institutions, hospitals, universitiesResearch organizations, academic institutions
Work Hours40+ hours/weekLess than 20 hours/week

Full Time Irb roles typically involve a standard 40+ hour workweek, requiring full-time commitment and consistent presence in research settings. Part Time Irb positions offer flexible hours, often less than 20 hours weekly, suitable for those balancing other responsibilities. Both roles require IRB certification and knowledge of research ethics, but the main difference lies in hours and work setting.

What are the typical responsibilities of a full-time IRB (Institutional Review Board) coordinator, and how does the role interact with researchers and regulatory bodies?

A full-time IRB coordinator is responsible for managing the ethical review process of research involving human subjects. This includes reviewing research proposals for compliance with federal regulations, facilitating IRB meetings, communicating required changes to researchers, and maintaining accurate records. Coordinators act as a critical liaison between researchers, IRB members, and regulatory agencies to ensure studies are conducted ethically and participants are protected. Daily tasks often involve document review, correspondence, and providing guidance to investigators, making strong communication and organizational skills essential.

What are the key skills and qualifications needed to thrive as a full-time IRB (Institutional Review Board) professional, and why are they important?

To thrive as a full-time IRB professional, you need a comprehensive understanding of research ethics, regulatory compliance (such as 45 CFR 46 and FDA regulations), and typically a background in life sciences or healthcare. Familiarity with electronic IRB management systems, compliance databases, and certifications like CIP (Certified IRB Professional) are commonly required. Strong analytical thinking, attention to detail, and effective communication are essential soft skills for reviewing protocols and collaborating with researchers. These competencies are critical for ensuring the protection of human research subjects and maintaining institutional and federal compliance.

What is a Full Time IRB?

A Full Time IRB (Institutional Review Board) professional is a specialist who works full-time to review, approve, and oversee research involving human subjects to ensure that ethical standards and regulatory requirements are met. They are responsible for protecting the rights and welfare of research participants by conducting ethical reviews, monitoring ongoing research, and providing guidance to researchers. Full Time IRB staff often work in universities, hospitals, or research institutions, and collaborate closely with researchers and compliance officers. Their role is essential to maintaining the integrity and safety of scientific research involving humans.
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What are the most commonly searched types of Irb jobs? The most popular types of Irb jobs are:
What states have the most Full Time Irb jobs? States with the most job openings for Full Time Irb jobs include:
Clinical Research Nurse

Clinical Research Nurse

TriHealth

Cincinnati, OH • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 24 days ago


TriHealth rating

7.3

Company rating: 7.3 out of 10

Based on 162 frontline employees who took The Breakroom Quiz

293rd of 871 rated healthcare providers


Job description

Job Description
***Clinical Research Nurse - Hatton Research - TriHealth Hatton Research Institute
Make a difference every day as a Registered Nurse at TriHealth Hatton Research Institute. Join a compassionate, servant-led team committed to excellence in patient care while working in a supportive, high-energy environment.
We offer career growth opportunities, and a comprehensive benefits package.
Apply today and grow your career with a team that truly values you.
Location:
  • Good Samaritan Hospital at 375 Dixmyth Avenue

Work Schedule:
  • Full-Time (80 hours bi-weekly)
  • Day shift
  • No weekends or holidays

Incentives & Benefits:
Comprehensive benefits package, including medical, dental, vision, paid time off, retirement plans, and tuition reimbursement. Please view our benefits page https://careers.trihealth.com/what-we-offer/benefits
Job Requirements:
  • Bachelor's Degree - Nursing (Required)
  • 2 - 3 years' experience in Clinical Nursing Critical Thinking (Required)
  • Proficient in Microsoft Office programs
  • Knowledge of clinical research
  • Registered Nurse Upon Hire Required
  • Basic Life Support (BLS) Upon Hire Required

Job Overview:
Acts as the clinical research nurse for research studies in which TriHealth participates. Acts as a liaison between Study Sponsors, Study Monitors, Principal Investigators, other physicians, hospital staff, and the Institutional Review Board (IRB) to coordinate the efforts necessary to efficiently and effectively conduct a clinical research study. Actively participate in the selection of studies TriHealth conducts, developing a process for implementation of the protocol, participating in the identification of potential subjects, participating in the informed consent process, enrolling subjects and accurately and thoroughly collecting and reporting data. Educates and coordinates the care of patients who are on research studies. Staff in this position can work at all sites where research is conducted within TriHealth. Travel between sites may be required. Staff in this position may be required to work in other research specialties other than the one for which they are hired. Staff in this position must be available to cover the needs of the department, which may be 7am-7pm. Staffing needs and hours are determined by amount and kind of studies the department has at any given time.
Job Responsibilities:
  • Demonstrates the ability to develop processes to facilitate implementation of the research protocol to provide effective and safe medical research to all subjects.
  • Demonstrates the ability to identify potential and/or actual issues, which may prohibit the accurate implementation of the research protocol and initiate interventions to avoid protocol violations and/or unsafe practice.

  • Demonstrates the ability to coordinate necessary activities between the Study Coordinators and the Principal Investigator.

  • Performs initial and ongoing assessments of research subjects and implements care directed towards optimal outcomes.

  • Plans care for research subjects/families based on assessment, standards of care, optimal outcomes and protocol requirements.

  • Implements and evaluates plan of care.

  • Performs technical skills according to policy and procedure and accepts TriHealth Standards.

  • Documents in medical records appropriately.

  • Comply with all IRB/FDA requirements in study submissions.

  • Assures compliance with IRB/FDA standards and deadlines in notification of subject randomization and enrollment.
  • Assures compliance with IRB/FDA standards and deadlines in completing Progress Reports.
  • Assures compliance with IRB/FDA standards and deadlines in reporting all deaths and adverse events within study subjects.

  • Assures compliance with IRB/FDA standards and deadlines in facilitating communication between study sponsor and designated IRB.

  • Appropriately and accurately assesses potential subjects for inclusion and exclusion criteria.

  • Keeps Case Report Forms complete and thorough using the IRB and FDA standards.

  • Supports hospital staff in complying with research protocols and works to minimize the impact on their workload.

  • Keeps queries and protocol violations that can be controlled to a minimum.

  • Responds appropriately and accurately to all queries in a timely fashion.

  • Demonstrates knowledge of available studies, screening potential patients for eligibility, guiding physicians and staff in needed timetables for appropriate randomization.

  • Participates in the identification and selection of good clinical protocols based on subject selection, safe medical practice and resource availability.

  • Attends training required by sponsoring organizations for specific protocols and/or attends meetings related to the initiation or on-going progress of a sponsored clinical trial.

  • Acts as the point person for audit staff coming into institution for a review prepares a written response with a plan of action to any major/minor deficiencies.

Working Conditions:
Bending - Rarely
Climbing - Rarely
Concentrating - Frequently
Continuous Learning - Frequently
Hearing: Conversation - Consistently
Hearing: Other Sounds - Frequently
Interpersonal Communication - Consistently
Kneeling - Occasionally
Lifting <10 Lbs. - Occasionally
Lifting 50+ Lbs. - Rarely
Lifting <50 Lbs. - Rarely
Pulling - Occasionally
Pushing - Occasionally
Reaching - Frequently
Reading - Frequently
Sitting - Frequently
Standing - Frequently
Stooping - Consistently
Talking - Frequently
Thinking/Reasoning - Consistently
Use of Hands - Frequently
Color Vision - Occasionally
Visual Acuity: Far - Consistently
Visual Acuity: Near - Consistently
Walking - Frequently
TriHealth SERVE Standards and ALWAYS Behaviors:
At TriHealth, we believe there is no responsibility more important than to SERVE our patients, our communities, and our fellow team members. To achieve our vision and mission, ALL TriHealth team members are expected to demonstrate and live the following:
Serve: ALWAYS...
• Welcome everyone by making eye contact, greeting with a smile, and saying "hello"
• Acknowledge when patients/guests are lost and escort them to their destination or find someone who can assist
• Refrain from using cell phones for personal reasons in public spaces or patient care areas
Excel: ALWAYS...
• Recognize and take personal responsibility to address and recover from service breakdowns when a customer's expectations have not been met
• Offer patients and guests priority when waiting (lines, elevators)
• Work on improving quality, safety, and service
Respect: ALWAYS...
• Respect cultural and spiritual differences and honor individual preferences.
• Respect everyone's opinion and contribution, regardless of title/role.
• Speak positively about my team members and other departments in front of patients and guests.
Value: ALWAYS...
• Value the time of others by striving to be on time, prepared and actively participating.
• Pick up trash, ensuring the physical environment is clean and safe.
• Be a good steward of our resources, using supplies and equipment efficiently and effectively, and will look for ways to avoid waste.
Engage: ALWAYS...
• Acknowledge wins and frequently thank team members and others for contributions.
• Show courtesy and compassion with customers, team members and the community
Job Keywords: Clinical Research, Research, Registered Nurse, Nurse

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About TriHealth

Sourced by ZipRecruiter

TriHealth provides unique opportunities from across disciplines in many different aspects including patient care, care coordination, education and management. We are unique because we know that team members who focus on our mission and values provide excellent patient care.

Industry

Health care and social assistance

Company size

10,000+ Employees

Headquarters location

Cincinnati, OH, US

Year founded

1995