Complete requisition forms, assemble kits for upcoming research visits, transport laboratory samples, and ensure samples are processed and shipped according to study specific guidelines, while tracking and maintaining research supplies.
May 17, 2020
Understand and adhere to the policies and procedures related to conduct of clinical trials as delineated in the Human Subject Research Manual.
June 06, 2020
Following the completion of protocol required visits, the completion of source documentation occurs and data entry within the required electronic data capture system occurs in a timely manner.
June 15, 2020
Assist the Principal Investigator (PI) with protocol development, revision, and study analysis.
June 25, 2020
Provide assistance upon request for the preparation of technical reports, abstracts, posters and manuscripts for submission to corporate and federal sponsors, conferences, and scientific journals.
July 10, 2020
Develop and maintain tools for study implementation, which may include data collection tools, study reference materials, and study specific orders.
August 04, 2020
Review protocol documents including abstracts, text and informed consent for relevant information.
August 07, 2020