Clinical Trial Manager at ICON managing trial operations, ensuring high - quality outcomes and compliance with trial protocols for clinical development in Beijing and Shanghai.
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
Job title
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