Top 8 Clinical research assistant Jobs in Dayton Oh

Clinical Research Coordinator
Wright State University —Dayton, OH
- Vital signs
- Mid-level
- Bachelor's degree
Clinical Research Coordinator
Dayton Center For Neurological Disorders Inc —Centerville, OH
- $25 - $35 an hour
- Full-time
- RN License
- Medical office experience
- Mid-level
- Profit sharing
- Disability insurance
Clinical Research Coordinator
Dayton Physicians, LLC —Kettering, OH
- No weekends
- Nursing
- Microsoft Outlook
- Mid-level
- Paid holidays
- Health insurance
Quick Apply
1d
Program Support Assistant
US Veterans Health Administration —Dayton, OH
- $52,339 - $68,043 a year
- Part-time
- Background check
- Psychiatry
- Pass drug screening
5d

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Research Assistant
Evolution Research Group —Columbus, OH
Founded in 2014, ERG has grown into a leading neuroscience clinical development company, with affiliate sites across the U.S. and deep expertise in clinical…
$20 an hour
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Assistant Clinical Research Coordinator
Dermatologists of Central States —Canal Winchester, OH
Assist with data entry, coding, and analysis as needed. Bachelor’s degree in a relevant field (e.g., Life Sciences, Nursing, Public Health).
$18 - $22 an hour
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12d

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Clinical Research Coordinator

Wright State University -
Dayton, OH

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Job Details

Qualifications

Specimen collection
Data preprocessing
Vital signs
Regulatory documents
Informed consent
Electronic health records (EHR) management
Research ethical considerations
Medical procedure assistance
Sample preparation
Operations coordination planning
Assisting with diagnostic tests and procedures
Assisting medical staff
Mid-level
State healthcare regulations
Patient safety
Research project coordination
ICH guidelines
Policy & process development
Bachelor's degree
Clinical data entry
Dermatology
Informed consent procedures implementation
Organizational skills
Clinical trial patient safety management
Implementing research protocols
Patient recruitment
Clinical research inspection readiness
Patient interaction
Research regulatory compliance
Data collection

Full Job Description

The Clinical Research Coordinator (CRC) supports the planning, implementation, execution, and completion of clinical and translational research studies conducted within the Pharmacology Translational Unit (PTU). The CRC works collaboratively with investigators, research nurses, sponsors, contract research organizations, and external clinical partners to ensure that research protocols are conducted in compliance with federal regulations, Good Clinical Practice (GCP), institutional policies, and study-specific requirements.

The CRC is responsible for participant scheduling, informed consent administration, data collection, source documentation, sample processing, monitoring visit preparation, and supporting overall study operations. This role requires strong organizational skills, attention to detail, and the ability to integrate research workflows within clinical settings.

Minimum Qualifications

Bachelor’s degree with 1 year of experience in clinical research OR in a clinical environment with direct interaction with patients, families, and healthcare staff. OR equivalent combination of education and experience.
Excellent oral and written communication skills.
Ability to work independently and collaboratively while maintaining regulatory and protocol timelines.
Strong organizational skills and a high level of attention to detail.
Demonstrated ability to prioritize responsibilities, manage competing deadlines, and troubleshoot operational issues.

Preferred Qualifications

Experience in dermatology research or other outpatient specialty research settings.
Knowledge of clinical research regulatory requirements (FDA, ICH-GCP, OHRP, IRB).
Experience supporting sponsor-initiated or investigator-initiated trials in an academic setting.
Familiarity with clinical billing practices and workflow coordination with clinic and hospital departments.
Experience with electronic data capture systems and electronic medical records.

Essential Functions and percent of time:

60% — Clinical Trial Coordination and Study Operations

Coordinate day-to-day study activities, including study startup, participant scheduling, visit coordination, monitoring visits, and study close-out.
Collaborate with investigators, research nurses, regulatory staff, and sponsors to ensure accurate and timely execution of protocol procedures.
Integrate research workflows into clinical settings across PTU-affiliated practice locations.
Serve as a liaison to investigators, medical staff, ancillary departments, and external partners to support study operations.
Ensure participant safety through ongoing communication, visit preparation, and protocol adherence.

25% — Participant Interaction, Enrollment, and Data Collection

Conduct participant screening, eligibility verification, and informed consent processes.
Support clinical procedures such as vital sign collection, dermatologic assessments, sample collection, and processing (as delegated and trained).
Maintain accurate and complete source documentation and complete case report forms or electronic data capture entries in a timely manner.

Essential Functions and percent of time (cont'd):

10% — Compliance, Documentation, and Monitoring Support

Ensure compliance with federal, state, institutional, and sponsor requirements.
Organize and maintain essential regulatory and study documentation.
Prepare for monitoring visits, audits, and sponsor inspections.
Assist with query resolution and data clean-up for interim and final database locks.

5% — Special Projects and PTU Support

Assist with quality assurance activities, workflow improvements, and study-related process development.
Contribute to team meetings, training sessions, and departmental initiatives.
Other duties as assigned.

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clinical research assistant jobs in dayton oh

Clinical Research Coordinator

Clinical Research Coordinator

Clinical Research Coordinator

Program Support Assistant

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