Clinical Data Specialist
Job Overview: Serve as a member of the project team with primary responsibility for conducting the clinical data review, query generation / resolution and reconciliation activities to support the Data
Life Science Jobs in India
Find Pharma, Biotech, Clinical Research & Medical Jobs on Bioksha
Found 11 jobs
Associate Clinical Data Manager
Job Overview: Data Management leadership on studies and take responsibility for the development of the project documentation, system set-up, data entry and data validation procedures and processes ass
Associate Clinical Data Manager (External Data)
Job Overview: Data Management leadership on studies and take responsibility for the development of the project documentation, system set-up, data entry and data validation procedures and processes ass
Senior Clinical Data Manager (External Data)
Job Overview: Data Management leadership on studies and take responsibility for the development of the project documentation, system set-up, data entry and data validation procedures and processes ass
Supplier Qualification Associate
Job Overview: The Associate plays a key role in our Supplier Qualification Office (SQO) within Global Regulatory Compliance & Quality Assurance in supporting the qualification of third-party clinical
Proposal Manager I
Summary of Responsibilities: Owns all aspects of the appropriate proposal process (text, quote, budget, and/or response to Requests for Information [RFIs]) for assigned opportunities (inclusive of man
Senior Centralized Study Spec
Summary of Responsibilities: Draft, review, negotiate, and finalize Clinical Trial Agreements (CTAs), confidentiality agreements, amendments, and related site contract documentation. Coordinate with s
Statistical Programmer 1 (DM SAS Listings Team)
Summary of Responsibilities: Provide Statistical Programming support for clinical trial projects. Develop, validate, and maintain SAS programs and outputs for the management, analysis, and reporting o
Regulatory Operations Expert
Job Overview: Scientific Writer with strong expertise in material science, analytical chemistry, and chemical principles (organic and inorganic) as applied to pharmaceutical formulation, manufacturing
Centralized Study Specialist II
Summary of Responsibilities: Draft, review, negotiate, and finalize Clinical Trial Agreements (CTAs), confidentiality agreements, amendments, and related site contract documentation. Coordinate with s
Safety Systems Specialist II, PSS
Job Overview: Assist with the overall Safety system implementation, support, configuration, and migration related activities. Responsible for providing this service to clients either as a support func
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