Project manager for phase I research
Site Project Manager
Responsible for managing an assigned set of multiple research protocols to ensure efficiency and regulatory compliance of the protocol, attending clinic as needed. Responsible for compilation, registration, and submission of data; monitors study compliance and maintains a system for effective data flow associated with research protocols. Supervises and directs a team of Clinical Operation Support Staff in the general conduct of studies at Lotus. Responsible for oversight of assigned teams for conducting studies as assigned in an efficient and well-organized manner.
Position supervises and directs Research assistants, CRC I and II staff and has the responsibility of workflow supervision of staff. Position requires extensive experience and judgment to accomplish study defined goals.
Bachelor’s degree; or 2-5 years related experience and/or training; or equivalent combination of education and experience. Minimum of 2-5 years of CRC experience required with two years supervisory experience, preferred. One (1) year experience working in a health care setting, preferably in research. Experience conducting vitals and EKGs required. Strong working knowledge of Clinical Research procedures and guidelines, required. Organizing and coordinating skills, teaching and facilitation skills, ability to assess training needs and objectives. Experience overseeing and coordinating the work of others.
Experience: