Regulatory Operations Specialist II
Job Overview: Responsible for responsible for managing laboratory instruments, ensuring compliance with regulatory standards, and supporting quality and validation activities in a cGMP environment. Su
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Regulatory Operations Specialist III
Job Overview: Responsible for the analytical support for the developmental projects/comparative dissolution projects and for the proper recording of information. Summary of Responsibilities: Respons
Regulatory Operations Specialist II
Job Overview: Responsible for the analytical support for the developmental projects/comparative dissolution projects and for the proper recording of information. Summary of Responsibilities: Respons
Programmer Analyst I (Clinical data managers / database designers)
Job Overview: Calling Clinical Data Managers / Database designers with strong experience in protocol interpretaion and edit checks specification keen to be trained in programming! Performs programming
Sr. Centralized Study Coordinator
Summary of Responsibilities: To complete Other duties/activities as assigned by study management team, but not limited to: Manage clinical systems and access management. Maintain study databases (CTMS
Safety Systems Specialist
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
Programming Lead
Summary of Responsibilities: Perform the role of the Lead Statistical Programmer. Plan, execute and oversee all programming activities on a study, including but not limited to, resource estimation, wo
Sr Clinical Data Specialist
Job Overview: Serve as a member of the project team with primary responsibility for clinical data review, query generation / resolution and reconciliation to support the delivery of clinical data acco
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
Senior Analyst, Real World Evidence
Job Overview: Providing programming and analysis support for Real World Evidence projects for Fortrea clients. Having good understanding of the various sources on Real World Data to be used in the ana
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
Sr. Stat. Prog. Specialist
Summary of Responsibilities: With sufficient experience assume the role of a Lead Statistical Programmer for CP studies only with support from senior programming staff. Plan, execute and oversee all p
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
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
Manager, CDM
Summary of Responsibilities: Based on forecast models, manage the resources to meet or exceed business Service Level Agreements. Supervise, Mentor, Evaluate and aid in staff development, career develo
Sr. Safety Writer
Job Overview: Lead the preparation and review of aggregate safety, risk management, signal detection, and benefit-risk evaluation reports. Be responsible for end-to-end report management, including pl
Statistical Programmer - RBQM programming
Key Responsibilities Develop and maintain R programs to support RBQM (Risk based Quality Management) for clinical trial data Collaborate with cross-functional teams to understand and implement projec
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