CLINICAL RESEARCH COORDINATOR II
Job Description
The University of Alabama at Birmingham (UAB), Department of Med - Cardiovascular Disease, is seeking a Clinical Research Coordinator II. The main focus of this position is to work on multi-site research by the VA. Therefore, all candidates must pass a VA background check and drug screen.
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
- Identifies, screens, and engages potential participants for vascular and cardiovascular studies.
- Conducts informed consent in compliance with regulations, explains study details clearly, and maintains communication with participants (including phone outreach) to support recruitment and retention.
- Coordinates study visits, follow-ups, and related activities across the study lifecycle.
- Tracks participant progress, sends reminders, and ensures adherence to protocols while maintaining strong communication with study subjects and clinical teams.
- Prepares and manages IRB submissions, including study initiation, modifications, amendments, and continuing reviews.
- Ensures compliance with federal, institutional, and GCP guidelines governing human subjects research.
- Performs accurate data entry and maintains both paper and electronic study records.
- Completes case report forms, manages REDCap databases, and ensures data integrity through organized, detailed documentation practices.
- Maintains compliance with all regulatory and protocol requirements, supports quality assurance activities, and ensures proper documentation.
- Collaborates effectively with investigators, clinical staff, and multi-site partners, including VA.
- Provides general operational support such as lab/specimen handling, study supplies management, and independent tasks.
- 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.
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