Clinical Research Coordinator - Cancer Control
The Ohio State University
•Onsite
About The Position
The Clinical Research Coordinator coordinates and performs daily clinical research activities in accordance with approved protocols administered by the Recruitment, Intervention and Survey Shared Resource, part of the Clinical Trials Office within The Ohio State University Comprehensive Cancer Center at The Ohio State University Wexner Medical Center.
Requirements
- Bachelor’s degree in biological sciences, health sciences, social sciences, or another medical field, or an equivalent combination of education and experience.
- One year of experience in a clinical research capacity.
- Computer skills.
- Ability to communicate effectively, face-to-face and in writing, with clinical staff, research participants, and outside collaborators.
Nice To Haves
- Knowledge of medical terminology.
- Clinical research certification from an accredited certifying agency.
- Experience using Microsoft Office software applications.
Responsibilities
- Assess patient records to identify patients eligible for specified clinical research protocols.
- Recruit, interview, and enroll patients.
- Obtain informed consent and ensure the consent process complies with regulatory and sponsor requirements.
- Educate patients and families about the purpose, goals, and processes of clinical studies.
- Coordinate scheduling and follow-through of patient care appointments, procedures, and diagnostic testing in accordance with study protocols.
- Assist with monitoring patients for adverse reactions to study treatment, procedures, or medication; notify appropriate clinical professionals to evaluate patient responses, determine the status of complications, and provide appropriate care.
- Document unfavorable responses and notify research sponsors and applicable regulatory agencies.
- Assist with collecting, extracting, coding, and analyzing clinical research data.
- Support compliance with Institutional Review Board (IRB), FDA, federal, state, and industry sponsor regulations.
- Assist with coordinating and preparing for external quality assurance and control reviews by the IRB, federal agencies, or industry sponsors.
- Participate in developing new research protocols and contribute to establishing study goals that meet protocol requirements.
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
