experience within the life science industry, preferably on the Sponsor side. Must have recent experience as the lead programmer...
Responsibilities: Support the planning, setup, and acquisition of external clinical data at the study level, assisting in managing study start-up, conduct, and closeout activities. Assist in creating external data transfer agreements, en...
Responsibilities: Leads all clinical data management activities for assigned clinical studies assuring all timelines are met with best quality. Responsible for overseeing creation and approval of DM study documentation by vendors/CROs (i...