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Senior Clinical Research Data Coordinator - Cancer Center - Clinical Trials Office

uic
Chicago, IL Full Time
POSTED ON 12/10/2024
AVAILABLE BEFORE 2/10/2025
Position Summary
This position is responsible for overseeing the collection, coordination, processing and quality control of clinical trial data. This includes pre and post research activities, internal and external to the clinical setting. Responsible for implementation and conducting data management and compliance of multiple research projects. Trains and mentors data coordinators and assists with maintenance of all data coordinator activities.

Duties & Responsibilities
  • Establish new processes to improve data coordinator workflow. Manage data coordinator workload and the onboarding of new protocols.
  • Collaborate with clinical and regulatory coordinators to document and report study patient enrollment, treatment, and follow-up into sponsor’s database, including protocol adherence, adverse events, and treatment outcomes.
  • Review and synthesize information from medical records (clinic notes, pathology reports, radiology reports, patient questionnaires, etc.) to extract industry, cooperative, and investigator-initiated trial data as specified by research protocol.
  • Prepare documents and coordinate the study team, including principal investigators and pharmacists, for internal and/or external compliance monitor review/audit. Participate in the review/audit process to ensure oncologic clinical trials can be conducted at UIC.
  • Oversee the handling, processing, and sending of protocol specific specimen requirements, kit management, and inventory supply
  • Perform other related duties and participate in special projects as assigned.
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