Clinical Research Coordinator Ii
Listed on 2026-02-12
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Healthcare
Clinical Research, Medical Science
Clinical Research Coordinator II
The University of Alabama at Birmingham (UAB), Dept of Optometry & Vision Science, is seeking a Clinical Research Coordinator II. The Clinical Research Coordinator II will assist with small- and large-scale clinical studies and trials in the field of eye- and vision-related research. Principal responsibilities include recruitment and retention efforts, data quality control, and regulatory compliance.
General Responsibilities- Serve as coordinator for studies and provide support to other team members within the confines of the protocol as directed.
- Support screening and participant eligibility determination, working with more team members to ensure compliance.
- Conduct activities in accordance with the protocol, regulations and Good Clinical Practice (GCP).
- 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.
Duties & Responsibilities
- Implement study participant recruiting and screening protocols.
- Collect, analyze, and enter data for clinical trials and ensure quality control.
- Complete enrollment logs, informed consent logs, and all other data forms with high accuracy and attention to detail.
- Perform general clerical duties (faxing, scanning, routing messages, coordinating the purchase of study supplies/materials).
- Enter data into REDCap and SPSS and summarize study data.
- Plan, organize, and coordinate multiple work assignments and establish and maintain effective working relationships with others.
- Establish rapport with study participants and maintain contact with enrolled participants.
- Train any assistants and volunteers who gather and enter data.
- Monitor compliance of study procedures with federal, state, and university regulations.
- Maintain eligibility forms and informed consent following IRB, Good Clinical Practice, and HIPAA regulations are followed.
- Effectively and professionally communicate sensitive information and maintain confidentiality.
- Perform other duties as assigned.
Annual Salary Range: $50,050 - $81,330
Bachelor’s degree in a related field and three (3) years of related experience required. Work experience may substitute for education requirement.
Preferences- Clinical trials research experience and regulatory experience.
- Ability to operate various office machines, including printers, computers, and various software packages.
- Interpersonal skills.
- Written and verbal communication skills.
- Detail-oriented.
- Prior research experience with human subjects, clinical trials, and regulatory experience.
- Experience using Windows, Microsoft Word, Microsoft Excel, Microsoft PowerPoint, Microsoft Outlook, and internet browsers.
- REDCap experience.
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 /titleix.
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