management, particularly in the oncology field. Requirements: Bachelor's degree in Life Sciences, Computer Science...
in development, validation, and management of the clinical study database throughout its life cycle, from CRF design, database...
(k) clearances and CE marking is required. Strong understanding of medical device product life cycle and regulatory requirements...
Responsibilities: Responsible for the oversight of all data management CRO activities supporting company's clinical programs from database start-up through database lock and CSR/submission. Serves as primary point of contact with the DM ...
Responsibilities: Effectively designs and codes SAS programs using BASE/SAS, SAS/STAT, SAS/GRAPH and SAS MACROS for assigned clinical projects(s) Produces and delivers CDISC and regulatory compliant SDTM, and ADaM standard datasets Crea...