CLINICAL RESEARCH COORDINATOR II
The University of Alabama at Birmingham (UAB), Med - Infectious Diseases, is seeking a Clinical Research Coordinator II.
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
- Assists 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 the coordination of lab and fieldwork.
- Serves as primary coordinator for studies and provides support to other team members within the confines of the protocol as directed.
- Prepares and maintains regulatory binders for all studies.
- Documents Adverse Events (AEs) and Serious Adverse Events (SAEs) as required by protocol and regulatory guidance.
- Completes and submits expedited SAE reports per protocol.
- Follows detailed SOPs for data collection and equipment use; trains others to do the same.
- Ensures study documentation is complete and compliant with study protocols.
- Oversees task assignments and ensures timely completion of responsibilities.
- Coordinates with departmental and financial teams for ordering, inventory management, patient payments, and budget development.
- Ensures accurate and timely data entry, collection, and reporting.
- Works with other research sites to ensure consistency across the study.
- Performs other duties as assigned.
Annual Salary Range
$50,050 - $81,330
Qualifications
Bachelor's degree in a related field and three (3) years of related experience required. Work experience may substitute for education requirement.
Preferences
- Clinical research experience.
- Clinical study project management experience.
- Experience with UAB's internal systems (IRAP, IRB, CIRB, etc).
- Study coordinator experience.
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