- Responsible for coordination of 20+ studies. In research projects oversees implementation of study procedures, and the collection and processing of data
- Performing phlebotomy, electrocardiograms, or monitor vital signs on study participants. Reports findings to supervisor
- Collects, labels, logs, processes, and ships biological specimens for analysis according to protocol to ensure proper transportation according to GCP and study SOP's
- Collecting data, confers with PI and forwards results to sponsor (internal or external
- Adheres to Good Clinical Practice and complies with regulatory and grant agency requirements. Follows protocol as developed. Keeps investigator or supervisor informed of developments
- Ensures availability of drug supplies and/or equipment for studies. Maintaining drug and equipment accountability logs
- Liaisons with agencies including: IRB, OCG, pharmaceutical companies, laboratories, and equipment and supply companies, as needed