Crystal Sheffield, Mph Email & Phone Number

Remote

Clinical Research Assistant for Eli Lilly’s TRAILBLAZER-ALZ Study

Charlotte, Nc, United States

Determines protocol-related needs to conduct the trial and orders supplies and equipment.Recruits and screens potential patients and obtains informed consent.Assists in providing patient education and benefits and risks of participating in a clinical drug trial.Designs organizational tools and forms to facilitate accurate data collection and recordkeeping.Conducts in-service programs, summarizes study schedule to assist in understanding and implementing a protocol.Schedules patient visits and laboratory and diagnostic test procedures.Coordinates drug shipments, storage, and accountability with pharmacy.Coordinates with Investigational Pharmacy for subjects to receive required drugs.Reviews trends, problems encountered, patient adverse events, and patient progress.Collect samples as needed and eligible.

Charlotte, North Carolina, United States

Coordinates the implementation and conduct of research projects ensuring adherence to research protocol requirements including: timely completion and communication of regulatory documents in accordance with GCP timelines.Serves as a liaison between investigators, research personnel, outside study personnel and central research administration offices to assist in protocol interpretation, enrollment and safety questions.Collaborates with primary investigator, sponsor and research staff to plan, conduct and evaluate project protocols, including research subject recruitment.Monitors and reports project status.Completes regulatory documents, data capture and monitoring plans.Develops and maintains knowledge of research protocol to coordinate the comprehensive and compliant execution of assigned protocols.

Cleveland, Ohio

Coordinates the implementation and conduct of research projects ensuring adherence to research protocol requirements including: timely completion and communication of regulatory documents in accordance with GCP timelines.Serves as a liaison between investigators, research personnel, outside study personnel and central research administration offices to assist in protocol interpretation, enrollment and safety questions.Collaborates with primary investigator, sponsor and research staff to plan, conduct and evaluate project protocols, including research subject recruitment.Monitors and reports project status.Completes regulatory documents, data capture and monitoring plans.Develops and maintains knowledge of research protocol to coordinate the comprehensive and compliant execution of assigned protocols.

New York, New York

Miami, Florida

Miami Shores

Tallahassee, Florida

Master'S Degree, Epidemiology

Bachelor'S Degree, Allied Health Sciences