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Clinical Research Program Manager Jobs in Ohio (NOW HIRING)

U.S. Renal Care

Clinical Research Coordinator

Toledo, OH · On-site

$21.75 - $28.75/hr

SUMMARY The Clinical Research Coordinator (CRC) is responsible for the coordination of daily ... Adheres to the USRC Research quality assurance program guidelines. * Travel to Investigator ...

U.S. Renal Care

Clinical Research Coordinator

Toledo, OH · On-site

$22.25 - $29.50/hr

Responsibilities SUMMARY The Clinical Research Coordinator (CRC) is responsible for the ... Adheres to the USRC Research quality assurance program guidelines. * Travel to Investigator ...

TriHealth

Clinical Research Coordinator

Cincinnati, OH · On-site

$23.25 - $31/hr

Coordinates and manages all components required for an organized multi-disciplinary team approach for the successful participation and completion of clinical research trials in TriHealth. Functioning ...

TriHealth

Clinical Research Nurse

Cincinnati, OH · On-site

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 ...

TriHealth

Clinical Research Nurse

Cincinnati, OH · On-site

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 ...

TriHealth, Inc.

Clinical Research Nurse

Cincinnati, OH · On-site

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 ...

TriHealth, Inc.

Clinical Research Coordinator

Cincinnati, OH · On-site

$23.25 - $31/hr

Coordinates and manages all components required for an organized multi-disciplinary team approach for the successful participation and completion of clinical research trials in TriHealth. Functioning ...

TriHealth

Clinical Research Nurse

Cincinnati, OH · On-site

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 ...

TriHealth

Clinical Research Coordinator

Cincinnati, OH · On-site

$23.25 - $31/hr

Coordinates and manages all components required for an organized multi-disciplinary team approach for the successful participation and completion of clinical research trials in TriHealth. Functioning ...

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All JobsClinical Research Program JobsClinical Research Program Manager JobsClinical Research Program Manager Jobs in Ohio

Clinical Research Program Manager information

See Ohio salary details

$42.3K

$88K

$142.1K

How much do clinical research program manager jobs pay per year?

As of Sep 12, 2026, the average yearly pay for clinical research program manager in Ohio is $88,038.00, according to ZipRecruiter salary data. Most workers in this role earn between $68,900.00 and $99,800.00 per year, depending on experience, location, and employer.

What does a clinical research program manager do?

A Clinical Research Program Manager oversees the planning, implementation, and management of clinical research studies within an organization. They coordinate research activities, ensure compliance with regulatory requirements, manage budgets, and supervise research staff. Their role is crucial in maintaining timelines, quality standards, and communication among stakeholders, including investigators, sponsors, and regulatory authorities. They also play a key part in developing study protocols and ensuring that research activities align with organizational goals.

What are the key skills and qualifications needed to thrive as a clinical research program manager?

To thrive as a Clinical Research Program Manager, you need a strong background in clinical research, project management, regulatory compliance, and often an advanced degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and certifications such as CCRP or PMP are typically required. Excellent leadership, organizational, and communication skills set standout managers apart, enabling them to coordinate teams and stakeholders effectively. These skills and qualifications are crucial for ensuring clinical studies meet regulatory standards, stay on schedule, and achieve high-quality outcomes.

What are some typical challenges faced by clinical research program managers in coordinating multi-site studies?

Clinical Research Program Managers often encounter challenges when coordinating multi-site studies, such as ensuring consistent protocol adherence across locations, managing data collection timelines, and addressing site-specific regulatory requirements. Effective communication and strong organizational skills are essential to keep all teams aligned and to resolve issues promptly. Additionally, the role frequently involves collaborating with investigators, sponsors, and regulatory bodies to maintain study integrity and ensure compliance.

What is the difference between Clinical Research Program Manager vs Clinical Research Coordinator?

AspectClinical Research Program ManagerClinical Research Coordinator
CredentialsBachelor's or higher in life sciences, often with project management certificationsTypically holds a bachelor's degree in health sciences or related field
Work EnvironmentOversees multiple studies, manages teams, and coordinates with stakeholdersHandles daily study activities, patient interactions, and data collection
Employer & Industry UsagePharmaceutical companies, CROs, academic institutionsHospitals, clinics, research sites
Search & Comparison IntentFocuses on management, oversight, and program coordinationFocuses on study-specific tasks and patient management

The Clinical Research Program Manager oversees multiple research projects, manages teams, and ensures compliance across studies. In contrast, the Clinical Research Coordinator handles the day-to-day activities of individual studies, including patient interactions and data collection. Both roles require relevant credentials but differ in scope and responsibilities.

What are the most commonly searched types of Clinical Research Program jobs in Ohio?

The most popular types of Clinical Research Program jobs in Ohio are:

What are popular job titles related to Clinical Research Program Manager jobs in Ohio?

For Clinical Research Program Manager jobs in Ohio, the most frequently searched job titles are:

What job categories do people searching Clinical Research Program Manager jobs in Ohio look for?

The top searched job categories for Clinical Research Program Manager jobs in Ohio are:

What cities in Ohio are hiring for Clinical Research Program Manager jobs?

Cities in Ohio with the most Clinical Research Program Manager job openings:

Clinical Research Program Manager jobs near you
Infographic showing various Clinical Research Program Manager job openings in Ohio as of September 2026, with employment types broken down into 1% Internship, 1% As Needed, 79% Full Time, 16% Part Time, and 3% Contract. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $88,038 per year, or $42.3 per hour.

Clinical Research Coordinator

Toledo, OH • On-site

U.S. Renal Care, Inc.
Health Care and Social Assistance • 1 - 5K employees
Learn more about U.S. Renal Care, Inc.external

$62K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 10 days ago

U.S. Renal Care rating

6.7

Company rating: 6.7 out of 10

Based on 95 frontline employees who took The Breakroom Quiz

Job description

Responsibilities
SUMMARY
The Clinical Research Coordinator (CRC) is responsible for the coordination of daily clinical trial activities. USRC has a research Partnership with the principal investigator (PI) and their physician practice. The local oversight and direction for activities related to the conduct of the clinical research is directed by the PI. The CRC will work collaboratively with the principal investigator (PI), the Sr. Clinical Research Coordinator (SCRC), the clinical site, sponsor(s), clinical research organization(s) (CROs), institutional review boards (IRBs), and study participants to ensure Execution of the clinical trial in accordance with the Study Protocol, the Food and Drug Administration (FDA), International Council for Harmonization of Technical Requirements for Pharmaceuticals for Human Use (ICH) and applicable state and local regulations. The CRC will assist the PI in protecting the rights, safety and welfare of all study participants.
Essential Duties and Responsibilities include the following. Other duties and tasks may be assigned.
  • Coordinate all aspects of participant care from screening through study completion as defined by the protocol and PI delegation.
  • Ensure and document that the informed consent process has occurred properly according to the Code of Federal Regulations (45 CFR part 46).
  • Assist in the process of maintaining and updating each study participant's source records, including collection of medical history, assessment of eligibility and documentation of all study related procedures and relevant information.
  • Promptly report adverse events, protocol deviations and unanticipated problems involving risk to human subjects or others to the PI, the Sponsor, the IRB and in accordance with the Federal Code of Regulations (21 CFR 312), with assistance as applicable.
  • Ensure thorough, individualized, protocol-based study subject education on all study processes including but not limited to informed consent, study participation obligations, appropriate use of investigational product (IP), IP side effects and safety, communication with study staff and research rights.
  • Provide timely and accurate exchange of participant information with the PI and research team as it pertains to study conduct and patient safety.
  • Adhere to the Health Insurance Portability and Accountability Act (HIPAA Privacy Rule) and protect participant confidentiality at all times.
  • Dispense, administer and instruct participants on proper use of the investigational product (IP) in accordance with the protocol, coordinator's scope of practice and at the direction of the PI, with assistance as needed.
  • Collaborate with the USRC clinical team. Participate in trial implementation, and ensure compliance with the study protocol by our clinical partners, with assistance as needed.
  • Perform accurate and timely data collection, source documentation, and entry into the USRC databases and sponsor Case Report Forms (CRFs)/ interactive web response systems (IWRS). Address queries and sponsor requests in a timely manner.
  • Aid in the coordination of long-term storage of research records in accordance with contractual requirements, with direction from the Director of Clinical Research.
  • Assist in the preparation of and attendance during site initiation meetings, monitoring visits, audit visits or regulatory authority inspections.
  • Responsible for the preparation and ongoing maintenance of Essential Documents (The Trial Master File). This includes those documents that will allow for the evaluation of the clinical trial and demonstrate compliance of the sponsor and PI with the study protocol and GCP. (Including but not limited to: Form FDA 1572, financial disclosures, laboratory certifications, protocol, investigator brochure, institutional review board (IRB) related documents, IND reports delegation of authority (DOA), study specific enrollment logs, monitoring reports, with assistance as needed.
  • Assists in the coordination of efforts of internal and external resources (industry partners, clinical research organizations) to ensure efficient trial selection, proper patient recruitment, achieving target enrollment goals and trial plan execution.
  • Fosters a patient-care culture that emphasizes patient safety and quality in all aspects.
  • Responsible for the patient stipend automated payment process including registration into the system and processing payments per the USRC policy and ongoing maintenance of payments during the trial.
  • Adheres to the USRC Research quality assurance program guidelines.
  • Travel to Investigator Meetings or similar research related meetings is required.
  • Travel may be required between dialysis facilities or nephrology practices within the community.
  • Develops a working knowledge of current clinical research practice standards and regulatory requirements. For example, but not limited to; (FDA Federal Code of Regulations Good Clinical Practice (GCP), Health Insurance Portability and Accountability Act (HIPPA), International Air and Transportation Association (IATA) - Shipping of Dangerous Goods. Maintains their industry standard licensures and certifications.
  • May provide training and oversight of Clinical Research Coordinators and/or Research Assistants.
  • Actively promotes GUEST customer service standards; develop effective relationships at all levels of the organization.
  • Participate in team concepts and promote a team effort; perform duties in accordance with company policies and procedures.
  • Participate in staff meetings as required.
  • Regular and reliable attendance is required for the job.
  • Actively promotes GUEST customer service standards; develops effective relationships at all levels of the organization.
  • Participates in team concepts and promote a team effort; performs duties in accordance with company policies and procedures.
  • Regular and reliable attendance is required for the job.

Qualifications
Qualifications/Requirements:
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily.
Requirements include:
  • Bachelor's degree in related field preferred.
  • (3) years of experience in clinical research required; nephrology experience preferred.
  • Basic knowledge of FDA regulations, IRB requirements and Good Clinical Practice.
  • Basic knowledge of kidney care and/or End-Stage Kidney Disease (ESKD) or similar field is a plus.
  • Strong verbal and written communication skills required.
  • Must have intermediate computer skills, including Microsoft Office (Word, Excel, Outlook and web based tools); proficiency in USRC applications required within 90 days of hire.

Benefit Details
All Full-Time employees are eligible for the following benefits:
* Medical / Pharmacy
* Dental
* Vision
* Voluntary benefits
* 401k with employer match
* Virtual Care
* Life Insurance
* Voluntary Benefits
* PTO
All Part Time employees are eligible for the following benefits:
* 401k with employer match
* PTO
Pay Range
USD $62,231.00 - USD $77,789.00 /Yr.

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