**YOUR TASKS AND RESPONSIBILITIES:** + Preparation & Review of start-up Documents: eCRF completion Guidelines, DMP, SAE reconciliation plan, Clinical Coding Plan + Preparation of Edit specification document (ESD), Test Plan and Data Entry Guideline + Screen design UAT + Edit checks UAT in CDMS as per ESD + Discrepancy Management + Support Data Manager in URS review for IWRS + Ensure timely completion of SAE reconciliation activities + Ensure timely completion of closeout activities including database lock + Preparation and update of Master Data Management File to ensure its completeness + Preparation & Review of Data Management Report **WHO YOU ARE:** + Pharmacy / Science Post-Graduate + At least 5 years of experience in the clinical data management domain in Pharma/CRO industry. Experience in, development of data management documents, development of validation plan, screen UAT, edit check UAT, clinical data query management etc. **Job Location:** Remote working job opportunity We provide equal employment opportunities for all current employees and applicants for employment. This policy means that no one will be discriminated against because of race, religion, creed, color, national origin, nationality, citizenship, ancestry, sex, age, marital status, physical or mental disability, affectional or sexual orientation, military or veteran status, generic predisposing characteristics or any other basis prohibited by law.