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Fda Nursing Jobs in Ohio (NOW HIRING)

Bachelor's Degree - Nursing (Required) * 2 - 3 years' experience in Clinical Nursing Critical ... Comply with all IRB/FDA requirements in study submissions. * Assures compliance with IRB/FDA ...

Bachelor's Degree - Nursing (Required) * 2 - 3 years' experience in Clinical Nursing Critical ... Comply with all IRB/FDA requirements in study submissions. * Assures compliance with IRB/FDA ...

Bachelor's Degree - Nursing (Required) * 2 - 3 years' experience in Clinical Nursing Critical ... Comply with all IRB/FDA requirements in study submissions. * Assures compliance with IRB/FDA ...

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Fda Nursing information

See Ohio salary details

$40.4K

$96.3K

$168.7K

How much do fda nursing jobs pay per year?

As of Aug 22, 2026, the average yearly pay for fda nursing in Ohio is $96,297.00, according to ZipRecruiter salary data. Most workers in this role earn between $66,500.00 and $116,000.00 per year, depending on experience, location, and employer.

What is FDA nursing?

An FDA Nursing job involves working within the U.S. Food and Drug Administration (FDA) to ensure public health and safety in relation to medical products, drugs, and clinical research. Nurses in these roles may conduct regulatory reviews, assess clinical trial data, or contribute to public health policies. They collaborate with scientists, policymakers, and healthcare professionals to ensure compliance with federal regulations. Their work helps ensure that medical treatments are safe, effective, and accessible to the public.

What types of projects or clinical studies do FDA nurses typically work on?

FDA Nurses often participate in clinical trials, post-market surveillance studies, and regulatory compliance reviews that involve investigational drugs, devices, or biologics. Their responsibilities may include monitoring patient safety, collecting data, ensuring protocol adherence, and preparing regulatory documentation for FDA submissions. The work environment often involves collaboration with research coordinators, physicians, regulatory specialists, and pharmaceutical companies. This role offers exposure to cutting-edge medical innovations, and experienced FDA Nurses can pursue advancement into clinical research management, regulatory affairs, or quality assurance roles.

What are the key skills and qualifications needed to thrive in the FDA nursing position, and why are they important?

To excel in FDA Nursing, candidates typically need a registered nursing degree, a valid RN license, and experience in clinical research or regulatory compliance. Familiarity with FDA regulations, Good Clinical Practice (GCP), electronic data capture systems, and report writing are highly valued. Attention to detail, strong organizational skills, and effective communication are important soft skills in this specialized area. These qualifications and qualities are vital to ensure accurate documentation, regulatory adherence, and the protection of patient safety in FDA-regulated environments.

What are popular job titles related to Fda Nursing jobs in Ohio?

For Fda Nursing jobs in Ohio, the most frequently searched job titles are:

Infographic showing various Fda Nursing job openings in Ohio as of August 2026, with employment types broken down into 3% As Needed, 61% Full Time, 14% Part Time, and 22% Contract. Highlights an 99% Physical, and 1% Remote job distribution, with an average salary of $96,297 per year, or $46.3 per hour.

Clinical Research Nurse

TriHealth

Cincinnati, OH • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 6 days ago


TriHealth rating

7.4

Company rating: 7.4 out of 10

Based on 175 frontline employees who took The Breakroom Quiz

268th of 891 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

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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