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Essential Duties and Responsibilities:
- Maintain a working knowledge of Protocol Coordinator responsibilities and work instructions.
- Attend monthly Protocol Coordinator meetings, Quarterly Senior Protocol Coordinator meetings, Monthly Trial Operations meetings, Epi meetings, and monthly ROR Committee meetings.
- Provide quality control reviews on protocols, informed consent documents (ICDs), and supplemental documents across Leagues, as assigned.
Qualifications:
- Two (2) years of relevant experience in quality control and/or clinical trial protocol development, including familiarity with clinical trial components such as IND and IRB process, study methodology, informed consent, eligibility and adverse events.
- Bachelor’s degree in Life Sciences or a related field, or substitute with four (4) additional years of relevant experience.
- Demonstrated success and skill at researching, analyzing, and evaluating scientific information.
COG Research Foundation, LLC
COG Research Foundation, LLC is the federal grantee organization for the Children's Oncology Group (COG). The COG unites over 12,000 experts in childhood cancer at more than 220 leading children’s hospitals, universities, and cancer centers across the United States, Canada, Australia, New Zealand, and Saudi Arabia.