All Activities relating to study start study conduct and study close out.
Preparation of below documents.
eCRF review
Preparing Trial derivation plans
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.
Good working Knowledge about the Databases (Medidata RAVE Oracle Clinical and Inform etc.)
Candidate should be flexible to shift
Excellent communication is required.
Employement Category:
Employement Type: Full timeIndustry: Bio Technology & Life SciencesFunctional Area: PharmaceuticalRole Category: Data ManagementRole/Responsibilies: Clinical Data Management (Team Lead)