Clinical Research Nurse
Cincinnati, OH · On-site
... Full-Time (80 hours bi-weekly) Day shift No weekends or holidays Incentives & Benefits ... Comply with all IRB/FDA requirements in study submissions. Assures compliance with IRB/FDA ...
Cincinnati, OH · On-site
... Full-Time (80 hours bi-weekly) Day shift No weekends or holidays Incentives & Benefits ... Comply with all IRB/FDA requirements in study submissions. Assures compliance with IRB/FDA ...
Cincinnati, OH · On-site
... Full-Time (80 hours bi-weekly) Day shift No weekends or holidays Incentives & Benefits ... Comply with all IRB/FDA requirements in study submissions. Assures compliance with IRB/FDA ...
Cincinnati, OH · On-site
Day shift * No weekends or holidays Incentives & Benefits: Comprehensive benefits package ... Comply with all IRB/FDA requirements in study submissions. * Assures compliance with IRB/FDA ...
Cincinnati, OH · On-site
Day shift * No weekends or holidays Incentives & Benefits: Comprehensive benefits package ... Comply with all IRB/FDA requirements in study submissions. * Assures compliance with IRB/FDA ...
Day shift * No weekends or holidays Incentives & Benefits: Comprehensive benefits package ... Comply with all IRB/FDA requirements in study submissions. * Assures compliance with IRB/FDA ...
Day shift * No weekends or holidays Incentives & Benefits: Comprehensive benefits package ... Comply with all IRB/FDA requirements in study submissions. * Assures compliance with IRB/FDA ...
Cincinnati, OH · On-site
Day shift * No weekends or holidays Incentives & Benefits: Comprehensive benefits package ... Comply with all IRB/FDA requirements in study submissions. * Assures compliance with IRB/FDA ...
Cincinnati, OH · On-site
Day shift * No weekends or holidays Incentives & Benefits: Comprehensive benefits package ... Comply with all IRB/FDA requirements in study submissions. * Assures compliance with IRB/FDA ...
Cincinnati, OH · On-site
... Full-Time (80 hours bi-weekly) Day shift No weekends or holidays Incentives & Benefits ... Comply with all IRB/FDA requirements in study submissions. Assures compliance with IRB/FDA ...
Cincinnati, OH · On-site
... Full-Time (80 hours bi-weekly) Day shift No weekends or holidays Incentives & Benefits ... Comply with all IRB/FDA requirements in study submissions. Assures compliance with IRB/FDA ...
Worcester, MA · On-site
$27.88/hr
... Day Shift Exempt Exempt/Non-Exempt Status Non Union Position-W00-Non Benefited Position Type ... Obtain consent of research participants in accordance with the IRB approved protocols and all ...
Worcester, MA · On-site
$27.88/hr
... Day Shift Exempt Exempt/Non-Exempt Status Non Union Position-W00-Non Benefited Position Type ... Obtain consent of research participants in accordance with the IRB approved protocols and all ...
Worcester, MA · On-site
$97K/yr
... Posted Date Day Shift Exempt Exempt/Non-Exempt Status Non Union Position -W60- Non Unit ... Report findings to the Principal Investigator, sponsor, and IRB when necessary * Review clinical ...
Worcester, MA · On-site
$97K/yr
... Posted Date Day Shift Exempt Exempt/Non-Exempt Status Non Union Position -W60- Non Unit ... Report findings to the Principal Investigator, sponsor, and IRB when necessary * Review clinical ...
Worcester, MA · On-site
$53/hr
... Posted Date Day Shift Exempt Exempt/Non-Exempt Status Non Union Position -W60- Non Unit ... Report findings to the Principal Investigator, sponsor, and IRB when necessary * Review clinical ...
Worcester, MA · On-site
$53/hr
... Posted Date Day Shift Exempt Exempt/Non-Exempt Status Non Union Position -W60- Non Unit ... Report findings to the Principal Investigator, sponsor, and IRB when necessary * Review clinical ...
Worcester, MA · On-site
$53/hr
... Posted Date Day Shift Exempt Exempt/Non-Exempt Status Non Union Position -W60- Non Unit ... Report findings to the Principal Investigator, sponsor, and IRB when necessary * Review clinical ...
Worcester, MA · On-site
$53/hr
... Posted Date Day Shift Exempt Exempt/Non-Exempt Status Non Union Position -W60- Non Unit ... Report findings to the Principal Investigator, sponsor, and IRB when necessary * Review clinical ...
Worcester, MA · On-site
$23.08/hr
... Day Shift Non Exempt Exempt/Non-Exempt Status Non Union Position -W60- Non Unit Professional ... Maintain all regulatory documentation, including local or central IRB and study data. Provide data ...
Worcester, MA · On-site
$23.08/hr
... Day Shift Non Exempt Exempt/Non-Exempt Status Non Union Position -W60- Non Unit Professional ... Maintain all regulatory documentation, including local or central IRB and study data. Provide data ...
... IRB). Duties includes obtaining regulatory approval for new protocols; maintaining approval for ... Regular day shift with occasional schedule variation to meet department needs. Daily contact with ...
... IRB). Duties includes obtaining regulatory approval for new protocols; maintaining approval for ... Regular day shift with occasional schedule variation to meet department needs. Daily contact with ...
Coordinates the day-to-day activities of the Institutional Review Board (IRB) office, including ... Wet or Slippery Surfaces = 0% Shift: Disclaimer: This is not intended, nor should it be construed ...
Coordinates the day-to-day activities of the Institutional Review Board (IRB) office, including ... Wet or Slippery Surfaces = 0% Shift: Disclaimer: This is not intended, nor should it be construed ...
... IRB). Duties includes obtaining regulatory approval for new protocols; maintaining approval for ... Regular day shift with occasional schedule variation to meet department needs. Daily contact with ...
... IRB). Duties includes obtaining regulatory approval for new protocols; maintaining approval for ... Regular day shift with occasional schedule variation to meet department needs. Daily contact with ...
... IRB). Duties includes obtaining regulatory approval for new protocols; maintaining approval for ... Regular day shift with occasional schedule variation to meet department needs. Daily contact with ...
... IRB). Duties includes obtaining regulatory approval for new protocols; maintaining approval for ... Regular day shift with occasional schedule variation to meet department needs. Daily contact with ...
... Day Shift * No Weekend or Holiday Commitment Benefits: TriHealth offers a comprehensive benefits ... Complies with all IRB/IACUC/FDA requirements in study submission to a central or local IRB.
... Day Shift * No Weekend or Holiday Commitment Benefits: TriHealth offers a comprehensive benefits ... Complies with all IRB/IACUC/FDA requirements in study submission to a central or local IRB.
Worcester, MA · On-site
$80K/yr
... Posted Date Day Shift Exempt Exempt/Non-Exempt Status Non Union Position -W60- Non Unit ... Obtain consent of research participants in accordance with the IRB approved protocols and all ...
Worcester, MA · On-site
$80K/yr
... Posted Date Day Shift Exempt Exempt/Non-Exempt Status Non Union Position -W60- Non Unit ... Obtain consent of research participants in accordance with the IRB approved protocols and all ...
Worcester, MA · On-site
$80K/yr
... Posted Date Day Shift Exempt Exempt/Non-Exempt Status Non Union Position -W60- Non Unit ... Obtain consent of research participants in accordance with the IRB approved protocols and all ...
Worcester, MA · On-site
$80K/yr
... Posted Date Day Shift Exempt Exempt/Non-Exempt Status Non Union Position -W60- Non Unit ... Obtain consent of research participants in accordance with the IRB approved protocols and all ...
Worcester, MA · On-site
$80K/yr
... Posted Date Day Shift Exempt Exempt/Non-Exempt Status Non Union Position -W60- Non Unit ... Obtain consent of research participants in accordance with the IRB approved protocols and all ...
Worcester, MA · On-site
$80K/yr
... Posted Date Day Shift Exempt Exempt/Non-Exempt Status Non Union Position -W60- Non Unit ... Obtain consent of research participants in accordance with the IRB approved protocols and all ...
Chicago, IL · On-site
$24 - $28/hr
Monday-Friday day shift (40 hours per week) Location: Onsite FLSA Classification: Non-Exempt ... Compile study information and submit initial, continuing and final reports to the IRB and/or ...
Quick apply
Chicago, IL · On-site
$24 - $28/hr
Monday-Friday day shift (40 hours per week) Location: Onsite FLSA Classification: Non-Exempt ... Compile study information and submit initial, continuing and final reports to the IRB and/or ...
Worcester, MA · On-site
$80K/yr
... Posted Date Day Shift Exempt Exempt/Non-Exempt Status Non Union Position -W60- Non Unit ... Obtain consent of research participants in accordance with the IRB approved protocols and all ...
Worcester, MA · On-site
$80K/yr
... Posted Date Day Shift Exempt Exempt/Non-Exempt Status Non Union Position -W60- Non Unit ... Obtain consent of research participants in accordance with the IRB approved protocols and all ...
$9.13 - $10.58
6% of jobs
$10.58 - $12.02
13% of jobs
$12.40 is the 25th percentile. Wages below this are outliers.
$12.02 - $13.46
23% of jobs
The median wage is $14.66 / hr.
$13.46 - $14.90
9% of jobs
$14.90 - $16.35
11% of jobs
$17.52 is the 75th percentile. Wages above this are outliers.
$16.35 - $17.79
16% of jobs
$17.79 - $19.23
12% of jobs
$19.23 - $20.67
4% of jobs
$20.67 - $22.12
2% of jobs
$22.12 - $23.56
2% of jobs
$23.56 - $25
2% of jobs
$9
$15
$25
| Aspect | Day Shift Irb | Day Shift Clinical Research Coordinator |
|---|---|---|
| Certifications | IRB approval, research compliance training | Good Clinical Practice (GCP), research ethics |
| Work Environment | Reviewing protocols, ensuring compliance, office setting | Participant interaction, site management, office/lab setting |
| Employer & Industry | Hospitals, research institutions, biotech firms | Hospitals, research centers, pharmaceutical companies |
Both roles involve research oversight and require knowledge of clinical protocols. The Day Shift Irb primarily focuses on reviewing and approving research protocols to ensure ethical standards, while the Day Shift Clinical Research Coordinator manages participant recruitment, data collection, and study coordination. Understanding these differences helps candidates choose the role that best fits their skills and career goals.
Cities with the most Day Shift Irb job openings:
The most popular types of Shift Irb jobs are:
States with the most job openings for Day Shift Irb jobs include:
The top searched job categories for Day Shift Irb jobs are:

Other
Medical, Dental, Vision, Retirement, PTO
Re-posted 29 days ago
7.4
Based on 175 frontline employees who took The Breakroom Quiz
270th of 887 rated healthcare providers
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.
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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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.
Health care and social assistance
10,000+ Employees
Cincinnati, OH, US
1995