Manager, Clinical Scientist, Hematology
Regeneron
Clinical Research Coordinator - Comprehensive Cancer Center
The Ohio State University, Main Campus
full-time
Posted on:
Location: Ohio • 🇺🇸 United States
Visit company websiteJob Level
Junior
Tech Stack
Assembly
About the role
- Assist with assessing patient records to identify patients who are eligible to participate in specified clinical research protocols
- Recruit, interview and enroll patients
- Obtain informed consent and ensure consent process is administered in compliance with regulatory and sponsor requirements
- Educate patients and families of purpose, goals, and processes of clinical study
- Coordinate scheduling and follow-through of patient care appointments, procedures, & other diagnostic testing in accordance with the study protocol
- Assist with monitoring patients for adverse reactions to study treatment, procedure, or medication and notifies appropriate clinical professionals to evaluate patient response, identify the status of complications, & provide the appropriate level of care
- Document unfavorable responses and notify research sponsors & applicable regulatory agencies
- Assist with collecting, extracting, coding, and analyzing clinical research data
- Support activities to ensure compliance with all Institutional Review Boards (IRB), FDA (Federal Drug Administration), federal, state, and industry sponsor regulations
- Assist with coordinating and preparing for external quality assurance and control reviews by IRB, federal or industry sponsors
- Participate in activities to develop new research protocols and contributes to the establishment of study goals to meet protocol requirements
Requirements
- Bachelor’s Degree in biological sciences, health sciences, social sciences, or other medical field or an equivalent combination of education and experience required.
- One year of experience in a clinical research capacity is required .
- Knowledge of medical terminology desired.
- Clinical research certification from an accredited certifying agency desired.
- Computer skills required with experience using Microsoft Office Software applications desired.
- Must be able to effectively communicate, both face-to-face and in writing, with clinical staff, research participants, and outside collaborators.
