The University of Alabama at Birmingham (UAB), Institute for Cancer Outcomes & Survivorship, is seeking a Clinical Research Coordinator I.
General Responsibilities
- To serve as coordinator for studies and provide support to other team members within the confines of the protocol as directed.
- To support screening and participant eligibility determination, working with more senior team members to ensure compliance.
- To conduct activities in accordance with the protocol, regulations and Good Clinical Practice (GCP).
- To assist with the study life cycle from start-up to closure, i.e., collecting and recording data, recruiting and performing follow-up with participants, scheduling visits and assisting in coordination of lab and fieldwork.
Key Duties & Responsibilities
- Recruits and retains patients for outcomes research by working with collaborating institutions and accessing large datasets cross-referencing multiple data points to find eligible patients.
- Works with research staff at collaborating sites to insure study integrity.
- Helps to train and mentor new clinical research staff members.
- Works with collaborators and collaborating sites regarding any protocol changes.
- Plays an active role in outcomes research project management.
- Ensures protocol compliance with intense monitoring of specific study requirements.
- Performs data management and data analysis as required by the research study.
- Works on special data management projects as assigned.
- Assists in preparation and submission of publications, presentations, literature searches and reference databases.
- Collects and delivers specimens for analysis using appropriate or specified equipment.
- Schedules protocol related tests and performs protocol specific clinical duties as required per the research study and monitors the progress of study participants.
- Maintains professional growth and development through seminars, workshops, and professional affiliations to keep abreast of the latest trends in the field of outcomes research.
- Manages an assigned set of multiple outcomes research protocols to assure efficiency and regulatory compliance of the protocol for the Institute for Cancer Outcomes and Survivorship.
- Attends clinic and assists in the lab as needed.
- Compiles, registers and submits data.
- Meets, schedules, and consents patients.
- Monitors study compliance and maintain a system for affective data flow associated with research protocols.
- Performs other duties as assigned.
Qualifications
High School diploma or GED required.
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