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Expert Clinical Data Manager

Mumbai, MH
Job Code:
  • Biotechnology & Science
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Job Details

Responsible and accountable for managing all Data Management deliverables with respect to cost, quality and timelines for all assigned programs, indications or trials managed within Clinical Data Management. Ensure consistently high quality data available for analysis and reporting Responsible for the Data Management (DM) start-up activities across assigned trials, indications or programs including electronic Case Report Form (eCRF) design and generation of the data handling and data review plans 2. Ensures consistency on the design of trials within a program/indication 3. Maintains standards within a program/indication 4. Identifies trends in the data and possible solutions for efficiencies 5. With support from Program Clinical Data Manager (PCDM) ensures study conventions, processes, knowledge sharing and best practice exist for all assigned trials 6. Skilled on a range of systems/tools in use by Novartis and by Contract Research Organization (CRO) partners and how to work with each accordingly 7. Effectively refines requirements for data validation based on metrics generated and les-sons learned from cleaning activities 8. Responsible for ongoing review of data, database maintenance & creation / maintenance of study documentation 9. Ensures the review of listings for quality, content, format and output 10. Supports & assists junior staff for assigned trials (e.g. raising data issues for Data Review Team (DRT) attention) 11. Responsible for the final review of data and finalization of the study documentation 12. Responsible for the final review of listings for quality, content, format and output 13. Tracks and reports status and progress for assigned trials, indications or programs. Is proactive to ensure timely deliverables (incl. Snapshots and interim/final locks). 14. Ensures appropriate tracking systems are kept up to date 15. Ensures creation of study specific project plans 16. Prepares feedback information about sites query performance and data entry compliance 17. Plans appropriately to ensure adherence to timelines, including assignment of workloads and identifying resource and timeline issues within and across programs 18. Interacts at International Clinical Teams (ICTs) and Biometrics and Data Management (BDM) Project Teams 19. Ensures adherence to GCP, DM standards, SOPs/Working Practices (WPs) and process guidelines 20. Able to effectively represent DM in SOP reviews and updates 21. Participates in Health Authority Inspections and assists in responding to requests for information from Health Authorities on DM related topics. 22. Responsible for managing all study documents required during a Regulatory or internal auditNovartis is an Equal Opportunity Employer.Minimum requirements.University or college degree in life science, computer science, pharmacy, nursing or equivalent relevant degree. Fluent English (oral and written). Ideally 6 years experience in Drug Development with at least 5 years' in Clinical Data Management
Additional Degree: B.Pharm. (Pharmacy) | B.Sc. (Science)

Experience: 6-10


Data Management/ Statistics | Documentation/ Medical Writing
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