This is a hybrid position, candidate must be a Medical Assistant with strong Administrative skills such paperwork processing, documentation, referrals, etc. Must have experience with blood draws and great attention to details.
The Clinical Research Coordinator (CRC) is a member of the study team that facilitates the day to day tasks associated with conducting a clinical trial. the CRC plays a critical role in facilitating, supporting, and coordinating daily clinical research study activities. The CRC works under the direct supervision of the
Clinical Trials Director (CTD).
Facilitate pre-study assessments, site qualification and initiation, monitoring visits, and study close out activities
Manage participant recruitment, (pre)screening, and enrollment
Educating participants and their family members on the details of the research study
Compliance with all Standard Operating Procedures related to each specific clinical trial/study.
Coordinating and assisting with research procedures, study visits, data collection(chief complaints, side effects and medications) and reporting, participant care and follow up
Coordinating with site clinical staff to ensure completion of study tasks
Phlebotomy- collect, process, and ship study laboratory specimens
Create and maintain documents
Identifying prescription medications patient is currently taking
Documentation & Regulatory Paperwork
Education and Experience:
3 Ways to Apply:
Preferred Medical Solutions