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Senior Clinical Research Assistant-Endocrinology, Diabetes and Metabolism

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Senior Clinical Research Assistant-Endocrinology, Diabetes and Metabolism

The Ohio State University logoThe Ohio State University
Columbus, USA
Posted: Sep 28, 2026

NL Highlights

Coordinate and perform clinical research activities for assigned studies, adhering to approved protocols.
Recruit, interview, enroll patients, and obtain informed consent.
Collect, process, and evaluate biological samples and administer patient assessments.

Details

Reference

R159717-2

Salary & Funding

Competitive academic stipend expected.

Duration

Regular

Contact Info

hr-accessibleapplication@osu.edu

Eligibility

Bachelor’s Degree in Biological Sciences, Health Sciences or medical field, or equivalent combination of education experience required.
At least one year of experience including at least 6 months patient interfacing experience in a clinical support capacity.
At least 6 months experience in a clinical research capacity required.
Proficient computer skills required.

Next Steps

1
Ensure you have all necessary documents available.
2
Review and update candidate profile information.
3
Complete the application process.
4
Final candidates are subject to successful completion of a background check.

Opportunity Overview

TITLE:

Senior Clinical Research Assistant-Endocrinology, Diabetes and Metabolism

Job Title:

Senior Clinical Research Assistant-Endocrinology, Diabetes and Metabolism

Department:

Medicine | IM Endocrinology, Diabetes and Metabolism

Senior Clinical Research Assistant within the Department of Internal Medicine, Division of Endocrinology- Accelerate with oversight from the College of Medicine (COM) Center for Clinical Research Management (CCRM); participates in data collection, maintenance and reporting and/or patient interfacing activities for a clinical research study.

Participates in coordinating and performing clinical research activities for assigned studies, including therapeutic studies involving SOC or FDA approved drugs/devices, in accordance with approved protocols; assists with assessing patient records to identify patients who are eligible to participate in specified clinical research protocols; recruits, interviews and enrolls patients; obtains informed consent and ensures consent process is administered in compliance to regulatory and sponsor requirements; educates patients and families of purpose, goals, and processes of clinical study; coordinates scheduling and follow-through of patient care appointments, procedures, and other diagnostic testing in accordance with study protocol; participates in the collection, processing and evaluation of biological samples; administers, evaluates and calculates standardized scoring of diagnostic, psychological or behavioral testing or questionnaires;

  • assists with training and onboarding new Clinical Research Assistants 2 and 3 as a preceptor.