Log in or sign up (free) to apply to this job.
About the role
Major purpose of the Job: -Reviewing overall data management activities for assigned studies. RESPONSIBILITY: Clinical Data Management: -Preparation of DMP (Data Management Plan), Data Validation Plan (DVP) and Self-Evident Correction Convention (SECC). -Preparing & Updating of SOPs. -Ensuring SOP compliance in project deliverables. -Generation of dummy data for User Acceptance Test (UAT) structure specification for validation process. -Follow up with Project Manager, CRA and Site Personnel and resolving their data management issues. -Performing final database QC activities. -Extraction of data from database in to excel sheet. -Performing database closure activities like Database -lock etc. -Testing of roles and responsibilities. -Providing study access to study personnel. -Performing Medical Coding for medical terms.
Ready to apply?
Create a free account to apply and tailor your resume to this role.
Apply on Cadila Pharmaceuticals Ltd