Data entry/tracking of clinical trial reports/documents/correspondence in the manner specified
in the Medicis Clinical Research SOP's related to study documents and in compliance with FDA
regulations & ICH guidelines. Must follow a format suitable for review by an FDA investigator.
Provide study maintenance support to investigator sites, CRA's and in-house teams. Coordinates
the management of study materials and relevant study documents. Requires the ability to
communicate effectively with busy physicians and support staff in accordance with the levels
of respect embodied in Medicis' core values.
Draft correspondence, letters, memos and various communications. Requires documentation of all
communications in a standardized format per Medicis Clinical Research SOP's. Must be able to
communicate effectively and professionally with physicians, investigative site personnel,
Medicis study teams, and upper management.