Inside Higher Ed
Clinical Research Coordinator - Comprehensive Cancer Center
Inside Higher Ed, Columbus, Ohio, United States, 43224
Job Title
Clinical Research Coordinator - Comprehensive Cancer Center
Department CCC | Clinical Trials Processing Lab
Location Remote (Ohio residency required)
Position Summary Clinical Research Coordinator to coordinate and perform daily clinical research activities for the Ohio State University’s Comprehensive Cancer Center (OSUCCC) Clinical Trials Processing Laboratory. Tasks include:
Coordinate correlative specimen study start‑up.
Review clinical trial protocols for feasibility and accuracy of correlative specimen needs.
Communicate with Clinical Trials Office Protocol implementation team on questions and revisions.
Review and edit laboratory manuals and study calendars.
Represent the CTPL at site study implementation and initiation meetings.
Communicate with sponsors and internal and external laboratories where samples are sent for analysis.
Create study‑specific educational materials for in‑services for clinical research staff.
Ensure all tasks are completed to allow studies to open in a timely manner.
Review amendments to existing protocols and communicate with sponsors and customers to update correlative specimen changes accurately.
Job Requirements
Bachelor’s Degree in Biological Sciences, Health Sciences, Social Sciences or other medical field, or equivalent combination of education and experience.
One year experience in a clinical research capacity, or knowledge in clinical research.
Knowledge of medical terminology desired.
Computer skills required.
Experience using Microsoft Software applications required.
Additional Information Research and Scholarship - Clinical Research - Individual Contributor - Specialized - S2 Experienced
Employment Details
Position Type: Regular
Scheduled Hours: 40
Shift: First Shift
Background Checks Final candidates are subject to successful completion of a background check. A drug screen or physical may be required during the post‑offer process.
Equal Employment Opportunity The university is an equal opportunity employer, including veterans and disability.
As required by Ohio Revised Code section 3345.0216, Ohio State will: educate students by means of free, open and rigorous intellectual inquiry to seek the truth; equip students with the opportunity to develop intellectual skills to reach their own, informed conclusions; not require, favor, disfavor or prohibit speech or lawful assembly; create a community dedicated to an ethic of civil and free inquiry, which respects the autonomy of each member, supports individual capacities for growth and tolerates differences in opinion; treat all faculty, staff and students as individuals, hold them to equal standards and provide equality of opportunity with regard to race, ethnicity, religion, sex, sexual orientation, gender identity or gender expression.
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Department CCC | Clinical Trials Processing Lab
Location Remote (Ohio residency required)
Position Summary Clinical Research Coordinator to coordinate and perform daily clinical research activities for the Ohio State University’s Comprehensive Cancer Center (OSUCCC) Clinical Trials Processing Laboratory. Tasks include:
Coordinate correlative specimen study start‑up.
Review clinical trial protocols for feasibility and accuracy of correlative specimen needs.
Communicate with Clinical Trials Office Protocol implementation team on questions and revisions.
Review and edit laboratory manuals and study calendars.
Represent the CTPL at site study implementation and initiation meetings.
Communicate with sponsors and internal and external laboratories where samples are sent for analysis.
Create study‑specific educational materials for in‑services for clinical research staff.
Ensure all tasks are completed to allow studies to open in a timely manner.
Review amendments to existing protocols and communicate with sponsors and customers to update correlative specimen changes accurately.
Job Requirements
Bachelor’s Degree in Biological Sciences, Health Sciences, Social Sciences or other medical field, or equivalent combination of education and experience.
One year experience in a clinical research capacity, or knowledge in clinical research.
Knowledge of medical terminology desired.
Computer skills required.
Experience using Microsoft Software applications required.
Additional Information Research and Scholarship - Clinical Research - Individual Contributor - Specialized - S2 Experienced
Employment Details
Position Type: Regular
Scheduled Hours: 40
Shift: First Shift
Background Checks Final candidates are subject to successful completion of a background check. A drug screen or physical may be required during the post‑offer process.
Equal Employment Opportunity The university is an equal opportunity employer, including veterans and disability.
As required by Ohio Revised Code section 3345.0216, Ohio State will: educate students by means of free, open and rigorous intellectual inquiry to seek the truth; equip students with the opportunity to develop intellectual skills to reach their own, informed conclusions; not require, favor, disfavor or prohibit speech or lawful assembly; create a community dedicated to an ethic of civil and free inquiry, which respects the autonomy of each member, supports individual capacities for growth and tolerates differences in opinion; treat all faculty, staff and students as individuals, hold them to equal standards and provide equality of opportunity with regard to race, ethnicity, religion, sex, sexual orientation, gender identity or gender expression.
#J-18808-Ljbffr