Description
Job Description:Assist in managing / supporting clinical studies; plan, implement, motivate, co-monitor, manage, and track clinical trials; assist in the supervision of field monitors, CROs; establish effective relationships with clinical investigators and staff, CROs, and vendors; participate in design/development of clinical trial protocols and preparation of clinical study/annual reports; work with data management to identify and resolve data discrepancies.
Job Requirements:
5+ years sponsor side pharmaceutical development experience. Strong global experience essential. Excellent vendor management and project management skills. RN desired. Available to travel up to 10% domestic and global.
Must be local to the SF Bay Area.
To find out more about Real please visit www.realstaffing.com