Job Role: All Activities relating to study start study conduct and study close out. Preparation of below documents. 1. eCRF review 2. Preparing Trial derivation plans 3. UAT of Edit checks Reports and DE screens Development of clinical data testing systems including design documentation implementation and report. Experience & Skills Required:
Relevant experience of above 4 years experience in Clinical Data Management from study start to close is mandatory.
Good working Knowledge about the Databases (Medidata RAVE Oracle Clinical and Inform etc.)
Employement Category:
Employement Type: Full timeIndustry: Bio Technology & Life SciencesFunctional Area: PharmaceuticalRole Category: Other PharmaRole/Responsibilies: Senior Associate / Team Lead CDM