Job Title

Experience Range: 8 – 14 yearsAbout the RolePrimarily responsible for quality and timely delivery of CP reports (Data Validation Listings, Reconciliation Reports, Coding Review, CRF Metrics, Patient Profiles and Narratives). Thorough understanding of End-to-End Drug Development Process. Good data understanding and Analytical skills. Keen knowledge on Data Management and Data cleaning process and willingness to work for adhoc requests. Having a skill set of Database Knowledge and flow, Study Protocol, CRF Design, Coding Dictionaries, Central vs Local lab concepts. Experience in debugging system level macros and modifying them for study level. Develop utility macros for reusability and efficiency. Coordinate work on multiple projects according to priorities. Communicate with project team/stakeholders/other departments and/or groups effectively.ResponsibilitiesAbility to program with and without specificationsReviewing and providing feedback on specifications when client provides themAbility to develop Macro from scratch or update existing macrosClient Level Interaction not restricted to cascading work but setting up a projectAbility to work independently and as part of a teamBeing open to new learnings and sharing with team membersExcellent communication skills [Written, Verbal, Interpersonal and organizational skills]Proficient in using SAS EG/Studio for programmingFamiliar with Unix environment and programmingExperience with additional programming languages (R/Python, Spotfire) will be an added advantage. QualificationsPost-graduate degree in statistics, computing, life science related field B.E/B techRequired SkillsGood data understanding and Analytical skills.Preferred SkillsExperience with additional programming languages (R/Python, Spotfire) will be an added advantageEqual Opportunity StatementWe are committed to diversity and inclusivity.