UA
UabCLINICAL RESEARCH COORDINATOR I
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Before you apply
Salary$44k – $71k
LocationUniversity
Also inThe University of Alabama at Birmingham (UAB), Med - Infectious Diseases
Typefull-time
SeniorityEntry
Company size10,000+ people
First seenOct 18, 2026 · 2w ago
Verified live2d ago
At a glanceSummarised by Seekless from the posting.
High school diploma or GED
Clinical research coordination experience
Ability to work under general supervision
Support screening and participant eligibility determination
Conduct activities in accordance with protocol, regulations and Good Clinical Practice (GCP)
Assist with the study life cycle from start-up to closure
Collect and record data, recruit and perform follow-up with participants
Schedule visits and assist in coordination of lab and fieldwork
Build collaborative relationships with implementation partners
Track and report site progress
Problem-solve study operations and implementation issues
Complete site visits and ensure study procedures are implemented per protocol
Coordinate meetings, set agendas, take notes
Attend to fiscal matters pertaining to study activities
Coordinate study-related supplies and purchases
Manage and train Research Assistants as needed
Support protocol development and SOPs
Perform occasional nursing duties such as phlebotomy and sample processing
Participate in informing participants of research results
Assist Program Director with additional roles or responsibilities
Bachelor's or Master's degree preferred
About the role
The University of Alabama at Birmingham (UAB), Med - Infectious Diseases, is seeking a Clinical Research Coordinator I.
Under general supervision, the Clinical Research Coordinator I performs duties related to initiating and implementing project activities. Supports project activities for the overall project but also specific to four teams: (1) Data and Evaluation; (2) AI Innovations; (3) Community Engagement; and (4) Communications, Media, and Policy.
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
1.
Builds collaborative relationships with implementation partners at different study sites.
2.
Tracks and reports site progress throughout the studies and problem-solves study operations and implementation issues.
3.
Identifies operational obstacles and finds solutions for proper study implementation and conduct.
4.
Completes site visits and ensures study procedures are being implemented as stated in the protocol.
5.
Meeting notes and coordinating/leading study meetings, keeping the studies moving forward and on track, including coordinating regular conference calls, setting agendas, and taking notes. Attending to fiscal matters pertaining to study activities as requested. Coordinating study-related supplies and purchases.
6.
Manages and trains Research Assistants as needed for specific activities.
7.
Supports protocol development and standard operating procedures (SOPs), Study Operations Manuals, etc. Participate in project training, maintain study certifications, etc.
8.
Perform occasional general nursing duties such as, but not limited to, phlebotomy, collection and processing of samples, and perform and/or assist with clinical procedures as necessary during the project visits.
9.
Participates in informing project participants of their research results, support compensation, etc. Support collecting, organizing, and maintaining data forms, collaborating with data personnel to ensure collected data is accurate and of high quality.
10.
Assists the Program Director with preparing reports, dissemination materials, etc. Assists the Program Director and Investigators with additional roles or responsibilities identified during project implementation
11.
Performs other duties as assigned.
Annual Salary Range: $43,890 - $71,320
Requirements
High School diploma or GED required.
Preferences
•
Bachelor’s or Master’s level degree preferred.
Legal
UAB is an Equal Employment/Equal Educational Opportunity Institution dedicated to providing equal opportunities and equal access to all individuals regardless of race, color, religion, ethnic or national origin, sex (including pregnancy), genetic information, age, disability, and veteran’s status. As required by Title IX, UAB prohibits sex discrimination in any education program or activity that it operates. Individuals may report concerns or questions to UAB’s Assistant Vice President and Senior Title IX Coordinator. The Title IX notice of nondiscrimination is located at uab.edu/titleix.