Clinical Data Specialist

Clinical Data Specialist 
Novartis - Hyderabad, Andhra Pradesh

Provide timely and professional ongoing management of clinical trial data by identifying and resolving errors and inconsistencies in eCRF data to ensure consistently high standard database(s) with respect to cost, quality and timelines. 1. Provide professional DM input on Clinical Trial Team(s) 2. Input to and review of clinical trial database design including User Acceptance Testing (UAT). 3. Provide input for the Validation and Analysis Plan (VAP) meeting for the clinical trial, which includes taking an active part in the meeting, providing input in writing the study specific validation checks and necessary reports to ensure high quality and consistent data. 4. Identify errors and inconsistencies; resolve them or initiate their resolution either via the field monitor or directly with the investigational site, to ensure high quality and timely database locks. 5. Review and contribute to preparation of protocols, specifically related to the data management section, visit schema and study design with supervision. 6. Prepare Case Report Forms (CRFs) and CRF completion Guidelines (CCGs), electronic or paper. For more info visit at mentioned link