Clinical Research Coordinator II at University of South Florida responsible for coordinating clinical research activities and ensuring participant data quality. Serving as main contact for sponsors and patients for specific research protocols.
About the role
- Clinical Research Coordinator I conducting clinical trials focused on health of African-American women. Involves data management, participant recruitment, and ensuring data integrity in health research.
Responsibilities
- Maintains data pertaining to research projects, completes source documents/case report forms, and performs data entry.
- Assists with patient recruitment.
- Attends study meetings.
- Orders and maintains equipment and supplies.
- Reviews medical records and/or conducts screenings for recruitment of study participants, performs interviews and QOL questionnaires.
- Collects study specimen according to protocol which may include phlebotomy, processing, and preparation for shipping.
- Coordinates services, schedules procedures, creates and maintains case packages, and monitors charges.
- Assists with quality assurance and tracks regulatory submissions.
- Performs related approved responsibilities as required.
Requirements
- High School Diploma or GED and three years of administrative support experience.
- Or two years of college in a scientific, health related, or business administration program and one year of admin support or customer service experience.
- Or be a licensed as a practical nurse (LPN) and one year admin support or one year of licensed practical nursing experience.
- Or a Bachelor's degree, Master's degree, MD or PhD in a scientific, health related or business administration program.
- Experience recruiting and enrolling Black or African American adults in research studies.
- Reside in the metro-Atlanta area.
- 2 years of research experience.
- High level of attention to detail for accurate data collection, documentation, and protocol adherence.
- Ability to identify issues, troubleshoot problems, and propose effective solutions in the context of clinical research.
- Comfort and professionalism in interacting with study participants, obtaining informed consent, and conducting study visits.
- Phlebotomy experience or certification (training and certification can be arranged after hiring).
- Highly organized.
- Strong written and oral communication skills.
- Reliable transportation.
Benefits
- Health and Safety Information Not Applicable
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