Senior Clinical Research Coordinator – Clinical Trials Office
The Ohio State University, Main Campus
full-time
Posted on:
Location Type: Remote
Location: Ohio • United States
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Job Level
About the role
- Serves as lead resource in the execution of assigned clinical research studies in accordance with approved protocols.
- Oversees & coordinates conduct of daily activities of research studies.
- Ensures informed consent authorization is obtained & administered in compliance to regulatory & sponsor requirements.
- Monitors subsite patients for adverse reactions to study treatment, procedure or medication and notifies appropriate clinical professional.
- Participates in extracting, coding, and analyzing clinical research data.
- Assists with preparation and submission of publications, research reports, and grant proposals.
Requirements
- Bachelor’s Degree in biological sciences, health sciences or medical field or an equivalent combination of education and experience required.
- Three to five years experience in a clinical research capacity conducting clinical research studies required.
- Experience or knowledge in specialty area preferred.
- Clinical research certification from an accredited certifying agency required.
- Computer skills required with experience using Microsoft Software applications desired.
Benefits
- Medical, dental and vision coverage, with Ohio State paying a significant portion of the cost.
- Paid time off, including sick and vacation time and 11 holidays.
- State retirement plan or an alternative retirement plan, both with generous employer contributions.
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
clinical researchdata extractiondata codingdata analysisinformed consent administrationadverse reaction monitoring
Soft Skills
leadershipcoordinationcommunication
Certifications
clinical research certification