CLINICAL RESEARCH COORDINATOR I

The University of Alabama at Birmingham (UAB), Dept of Optometry & Vision Science, is seeking a Clinical Research Coordinator I.

The Clinical Research Coordinator I 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

• 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. Collects and records preliminary data for clinical research programs.
2. Recruits and performs follow-up with research participants as protocols outline.
3. Schedules visits according to research protocols.
4. Assists in the coordination of lab and fieldwork.
5. Prepares for study monitoring visits.
6. Assists with correcting findings.
7. Assists with the completion of Case Report Forms (CRF) according to protocol.
8. Assists with the development of protocols and standard operating procedures (SOPs) for data quality assurance.
9. Performs general clerical duties (faxing, scanning, routing messages, coordinating the purchase of study supplies/materials).
10. May perform a variety of medical procedures under supervision.
11. May assist in compiling, editing, and proofing written reports for both internal and external administrative offices.
12. May perform data analysis using a variety of software packages.
13. Uses Electronic Data Capture (EDC) systems necessary for operations under supervision
14. Performs other duties as assigned.

Annual Salary Range: $43,890 - $71,320

Qualifications

High School diploma or GED required.

Preferences

• Clinical trials research experience, 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 and clinical trials, and regulatory experience.
• Experience using Windows, Microsoft Word, Microsoft Excel, Microsoft PowerPoint, Microsoft Outlook, and internet browsers.