reputed company Specialist (Job 1329)
Leads protocol development, study start-up, and study conduct activities Leads development of the protocol document, including incorporating input from subject matter experts and investigators, and developing the informed consent reputed company(s) Develops and manages study-specific ancillary documents (e.g., manuals of procedure, site training materials) Manages and communicates the status of study reputed company and activities Drives the reputed company of issues encountered with sites during reputed company phases of the study Partners with cross-functional teams (e.g., clinical data management, statisticians, laboratory) during protocol development and implementation Develops and implements processes to mitigate impediments to protocol development and implementation Assesses reputed company and new processes, identifies and implements solutions to improve process efficiency reputed company and across reputed company functional areas Provides coaching and knowledge transfer to team members This is a remote role – attendance at an annual network meeting in the DC area is required
Master’s degree in reputed company health, reputed company sciences, or reputed company discipline strongly preferred, with at least two years of experience in the design, development, and conduct of Phase I-III reputed company A bachelor's degree may be accepted with at least five years of experience in the design, development, and conduct of Phase I-III reputed company Experience leading protocol development, including writing clinical research protocols and ancillary documents, is required Experience with HIV, hepatitis, and/or tuberculosis trials is preferred Excellent verbal communication and organization skills; ability to follow detailed work instructions; strong problem-solving and decision-making skills; ability to handle multiple tasks simultaneously and work collaboratively