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: Responsible for leading study team through end-to-end regulatory submission activities. Hands-on SAS programming for creation and QC of clinical Tables, Listings and Graphs. Perform validation and QC of the programs,...
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...