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 ...
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 ...
... Board (IRB) or Institutional Animal Care and Use Committee (IACUC), and provide technical ... PPO medical plan, available day one at no cost for full-time employee-only coverage * 100% coverage ...
... Board (IRB) or Institutional Animal Care and Use Committee (IACUC), and provide technical ... PPO medical plan, available day one at no cost for full-time employee-only coverage * 100% coverage ...
Research Protections Coordinator
Chicago, IL · On-site
$38K - $48K/yr
What You'll Do: - Coordinate the intake, tracking, and processing of IRB, IBC, and IACUC ... Generous paid time off, sick time, holidays, floating holidays, and more! * Full-Time Benefits For ...
Research Protections Coordinator
Chicago, IL · On-site
$38K - $48K/yr
What You'll Do: - Coordinate the intake, tracking, and processing of IRB, IBC, and IACUC ... Generous paid time off, sick time, holidays, floating holidays, and more! * Full-Time Benefits For ...
These are for IRB-approved protocols as required by federal regulations and internal policy ... EXPERIENCE - 3 Years of Experience Employment Type: FULL_TIME
These are for IRB-approved protocols as required by federal regulations and internal policy ... EXPERIENCE - 3 Years of Experience Employment Type: FULL_TIME
PS Clinical Research Coord
Salt Lake City, UT · On-site
$23.50 - $31.25/hr
Yes Standard Hours per Week 40 Full Time or Part Time? Full Time Shift Day Work Schedule Summary ... Coordinates with study sponsor, investigator and IRB to complete study closure activities. 9. ...
PS Clinical Research Coord
Salt Lake City, UT · On-site
$23.50 - $31.25/hr
Yes Standard Hours per Week 40 Full Time or Part Time? Full Time Shift Day Work Schedule Summary ... Coordinates with study sponsor, investigator and IRB to complete study closure activities. 9. ...
Research Compliance Specialist
Chicago, IL · On-site +1
$68K - $70K/yr
... 600 full-time faculty and staff. As an institution, The Chicago School is deeply committed to ... Conduct for-cause audits authorized by the IRB or institutional official. * Conduct periodic ...
Research Compliance Specialist
Chicago, IL · On-site +1
$68K - $70K/yr
... 600 full-time faculty and staff. As an institution, The Chicago School is deeply committed to ... Conduct for-cause audits authorized by the IRB or institutional official. * Conduct periodic ...
Regulatory Associate
Dallas, TX · On-site
... Board (IRB) submissions, performance site reviews, and other required regulatory approvals, to ... PPO medical plan, available day one at no cost for full-time employee-only coverage * 100% coverage ...
Regulatory Associate
Dallas, TX · On-site
... Board (IRB) submissions, performance site reviews, and other required regulatory approvals, to ... PPO medical plan, available day one at no cost for full-time employee-only coverage * 100% coverage ...
Regulatory Analyst - Remote
Miami, FL · On-site +1
The University of Miami/UHealth Department of SCCC has an exciting opportunity for a Full Time ... Initial IRB application * Amendments / modifications * Reportable new information * Protocol ...
Regulatory Analyst - Remote
Miami, FL · On-site +1
The University of Miami/UHealth Department of SCCC has an exciting opportunity for a Full Time ... Initial IRB application * Amendments / modifications * Reportable new information * Protocol ...
Regulatory Analyst - Remote
Miami, FL · On-site +1
The University of Miami/UHealth Department of SCCC has an exciting opportunity for a Full Time ... Initial IRB application * Amendments / modifications * Reportable new information * Protocol ...
Regulatory Analyst - Remote
Miami, FL · On-site +1
The University of Miami/UHealth Department of SCCC has an exciting opportunity for a Full Time ... Initial IRB application * Amendments / modifications * Reportable new information * Protocol ...
PS Clinical Research Coord
Murray, UT · On-site
$59K - $65K/yr
Yes Standard Hours per Week 40 Full Time or Part Time? Full Time Shift Day Work Schedule Summary ... Coordinates with study sponsor, investigator and IRB to complete study closure activities. 9. ...
PS Clinical Research Coord
Murray, UT · On-site
$59K - $65K/yr
Yes Standard Hours per Week 40 Full Time or Part Time? Full Time Shift Day Work Schedule Summary ... Coordinates with study sponsor, investigator and IRB to complete study closure activities. 9. ...
Regular Full-Time Location: Glassboro, New Jersey Categories: Managerial The Director of Research ... The position oversees the Institutional Review Board (IRB), Institutional Animal Care and Use ...
Regular Full-Time Location: Glassboro, New Jersey Categories: Managerial The Director of Research ... The position oversees the Institutional Review Board (IRB), Institutional Animal Care and Use ...
Regulatory Associate
Dallas, TX · On-site
... Board (IRB) submissions, performance site reviews, and other required regulatory approvals, to ... PPO medical plan, available day one at no cost for full-time employee-only coverage * 100% coverage ...
Regulatory Associate
Dallas, TX · On-site
... Board (IRB) submissions, performance site reviews, and other required regulatory approvals, to ... PPO medical plan, available day one at no cost for full-time employee-only coverage * 100% coverage ...
Clinical Research Associate I, Medicine
Buffalo, NY · On-site
$60K - $80K/yr
... Full-Time Appointment Term Salary Grade E.99 Posting Detail Information Position Summary The ... Obtain informed consent according to IRB and regulatory requirements * Independently prioritize ...
Clinical Research Associate I, Medicine
Buffalo, NY · On-site
$60K - $80K/yr
... Full-Time Appointment Term Salary Grade E.99 Posting Detail Information Position Summary The ... Obtain informed consent according to IRB and regulatory requirements * Independently prioritize ...
Regulatory Associate
Dallas, TX · On-site
... Board (IRB) submissions, performance site reviews, and other required regulatory approvals, to ... PPO medical plan, available day one at no cost for full-time employee-only coverage * 100% coverage ...
Regulatory Associate
Dallas, TX · On-site
... Board (IRB) submissions, performance site reviews, and other required regulatory approvals, to ... PPO medical plan, available day one at no cost for full-time employee-only coverage * 100% coverage ...
Regulatory Associate
Dallas, TX · On-site
... Board (IRB) submissions, performance site reviews, and other required regulatory approvals, to ... PPO medical plan, available day one at no cost for full-time employee-only coverage * 100% coverage ...
Regulatory Associate
Dallas, TX · On-site
... Board (IRB) submissions, performance site reviews, and other required regulatory approvals, to ... PPO medical plan, available day one at no cost for full-time employee-only coverage * 100% coverage ...
* Prepare and/or coordinate IRB and other required submissions and approvals of new phase I-III and other protocols for industry, investigator-initiated, and national cooperative group studies in ...
New
* Prepare and/or coordinate IRB and other required submissions and approvals of new phase I-III and other protocols for industry, investigator-initiated, and national cooperative group studies in ...
New
Regulatory Associate
Dallas, TX · On-site
... Board (IRB) submissions, performance site reviews, and other required regulatory approvals, to ... PPO medical plan, available day one at no cost for full-time employee-only coverage * 100% coverage ...
Regulatory Associate
Dallas, TX · On-site
... Board (IRB) submissions, performance site reviews, and other required regulatory approvals, to ... PPO medical plan, available day one at no cost for full-time employee-only coverage * 100% coverage ...
Notifies IRB of protocol amendments, safety reports, and reportable information in compliance with applicable regulations. * Implements research protocols and monitors participant and study team ...
Notifies IRB of protocol amendments, safety reports, and reportable information in compliance with applicable regulations. * Implements research protocols and monitors participant and study team ...
Regulatory Associate
Dallas, TX · On-site
... Board (IRB) submissions, performance site reviews, and other required regulatory approvals, to ... PPO medical plan, available day one at no cost for full-time employee-only coverage * 100% coverage ...
Regulatory Associate
Dallas, TX · On-site
... Board (IRB) submissions, performance site reviews, and other required regulatory approvals, to ... PPO medical plan, available day one at no cost for full-time employee-only coverage * 100% coverage ...
Director of Research Compliance
Glassboro, NJ · On-site
$108K - $120K/yr
Regular Full-Time Location: Glassboro, New Jersey Categories: Managerial The Director of Research ... The position oversees the Institutional Review Board (IRB), Institutional Animal Care and Use ...
Director of Research Compliance
Glassboro, NJ · On-site
$108K - $120K/yr
Regular Full-Time Location: Glassboro, New Jersey Categories: Managerial The Director of Research ... The position oversees the Institutional Review Board (IRB), Institutional Animal Care and Use ...
Full Time Irb information
See salary details
$62K - $92.7K
6% of jobs
$92.7K - $123.5K
0% of jobs
$123.5K - $154.2K
0% of jobs
$154.2K - $184.9K
0% of jobs
$184.9K - $215.6K
4% of jobs
$215.6K - $246.4K
2% of jobs
$246.4K - $277.1K
1% of jobs
$307.8K is the 25th percentile. Wages below this are outliers.
$277.1K - $307.8K
11% of jobs
$307.8K - $338.5K
22% of jobs
The median wage is $342K / yr.
$338.5K - $369.3K
28% of jobs
$369.3K - $400K
25% of jobs
$62K
$330.1K
$400K
How much do full time irb jobs pay per year?
What is the difference between Full Time Irb vs Part Time Irb?
| Aspect | Full Time Irb | Part Time Irb |
|---|---|---|
| Credentials | IRB certification, research ethics training | IRB certification, research ethics training |
| Work Environment | Office, research institutions, hospitals | Flexible, part-time settings, remote options |
| Employer & Industry | Research institutions, hospitals, universities | Research organizations, academic institutions |
| Work Hours | 40+ hours/week | Less 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 coordinator, and how does the role interact with researchers and regulatory bodies?
What are the key skills and qualifications needed to thrive as a full time IRB professional, and why are they important?
What is a full time IRB?

Full-time
Medical, Dental, Vision, Retirement, PTO
Re-posted 26 days ago
TriHealth rating
7.4
Based on 175 frontline employees who took The Breakroom Quiz
268th of 887 rated healthcare providers
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 Apply Apply (Existing Employee)
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About TriHealth
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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