The Ohio State University
Clinical Research Coordinator - Comprehensive Cancer Center
The Ohio State University, Columbus, Ohio, United States, 43224
Job Title: Clinical Research Coordinator – Comprehensive Cancer Center
Department: CCC | Clinical Trials Processing Lab
Location: Remote
Position Type: Regular – 40 hours per week
Shift: First Shift
Position Summary Clinical Research Coordinator to coordinate and perform daily clinical research activities for OSUCCC’s Clinical Trials Processing Laboratory; functioning as an integral part of a team working with multi-disciplinary programs; coordinates correlative specimen study start‑up; reviews clinical trial protocols for feasibility and accuracy of correlative specimen needs; communicates with Clinical Trials Office Protocol implementation team on questions and revisions; reviews and edits laboratory manuals and study calendars; represents the CTPL at site study implementation and initiation meetings; communicates with sponsors as well as internal and external laboratories where samples are sent for analysis; creates study specific educational materials for in‑services for clinical research staff; ensures all tasks are completed to allow studies to open in a timely manner; reviews amendments to existing protocols and communicates with sponsors as well as internal and external customers to ensure changes to correlative specimen needs are updated accurately.
Job Requirements
Bachelor’s Degree in Biological Sciences, Health Sciences, Social Sciences or other medical field, or equivalent combination of education and experience required.
One year experience in a clinical research capacity or knowledge in clinical research required.
Knowledge of medical terminology desired.
Computer skills required; experience using Microsoft Software applications required.
This position will require occasional onsite presence, so Ohio residency is required.
Final candidates are subject to successful completion of a background check. A drug screen or physical may be required during the post‑offer process.
Thank you for your interest in positions at The Ohio State University and Wexner Medical Center. Once you have applied, the most updated information on the status of your application can be found by visiting the Candidate Home section of this site. Please view your submitted applications by logging in and reviewing your status. For answers to additional questions please review the frequently asked questions.
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.
Research and Scholarship - Clinical Research - Individual Contributor - Specialized - S2 Experienced
#J-18808-Ljbffr
Department: CCC | Clinical Trials Processing Lab
Location: Remote
Position Type: Regular – 40 hours per week
Shift: First Shift
Position Summary Clinical Research Coordinator to coordinate and perform daily clinical research activities for OSUCCC’s Clinical Trials Processing Laboratory; functioning as an integral part of a team working with multi-disciplinary programs; coordinates correlative specimen study start‑up; reviews clinical trial protocols for feasibility and accuracy of correlative specimen needs; communicates with Clinical Trials Office Protocol implementation team on questions and revisions; reviews and edits laboratory manuals and study calendars; represents the CTPL at site study implementation and initiation meetings; communicates with sponsors as well as internal and external laboratories where samples are sent for analysis; creates study specific educational materials for in‑services for clinical research staff; ensures all tasks are completed to allow studies to open in a timely manner; reviews amendments to existing protocols and communicates with sponsors as well as internal and external customers to ensure changes to correlative specimen needs are updated accurately.
Job Requirements
Bachelor’s Degree in Biological Sciences, Health Sciences, Social Sciences or other medical field, or equivalent combination of education and experience required.
One year experience in a clinical research capacity or knowledge in clinical research required.
Knowledge of medical terminology desired.
Computer skills required; experience using Microsoft Software applications required.
This position will require occasional onsite presence, so Ohio residency is required.
Final candidates are subject to successful completion of a background check. A drug screen or physical may be required during the post‑offer process.
Thank you for your interest in positions at The Ohio State University and Wexner Medical Center. Once you have applied, the most updated information on the status of your application can be found by visiting the Candidate Home section of this site. Please view your submitted applications by logging in and reviewing your status. For answers to additional questions please review the frequently asked questions.
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.
Research and Scholarship - Clinical Research - Individual Contributor - Specialized - S2 Experienced
#J-18808-Ljbffr