Description:
Working with patients that are in active treatment that they are seeing in addition to follow up appointments.
Heavy into phase 1, although will be working in phases 1-4.
20% administrative responsibilities as a leader directly related to work flow, process improvement and protocol review.
Responsible for independently running and operating multiple research protocols
Determines facility and supply needs required for set-up and implementation of research protocols
Assists in identifying study related procedures for the project budget.
Prepares for and is present for sponsor representative site visits.
Provides regional leadership for assigned research.
Be able to perform all of the duties of the Clinical Research Coordinator.
Trains and/or may supervise Clinical Research Assistants and/or Clinical Research Coordinators.
Assists with preparing for and conducting qualification, study initiation, interim monitoring, and close-out visits at investigator sites in conjunction with the Clinical Research Manager.
Mentor and lead others
Qualifications:
3 years of oncology CRC experience
5 years total research experience
Associates degree with experience required, Bachelors preferred
Must be a Certified Clinical Research Coordinator (CCRC-ACRP)
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