Veeva Programmer
Job Overview: Assist in the development and implementation of solutions to DM service issues and concerns regarding Medidata RAVE, Oracle Inform, CRF Design, and Data Capture or imaging activities, in
Life Science Jobs in India
Find Pharma, Biotech, Clinical Research & Medical Jobs on Bioksha
Found 23 jobs
TMF Reviewer II
Job Overview: Responsible for performing TMF review of electronic Trial Master Files (eTMF), Trial, Country, and Site artifacts for clinical studies in support of sponsors services contracts and inter
Senior Technical Designer
Job Overview: Responsibility for delivering EDC design and specifications within the scope of assigned projects to achieve project integrity and the delivery of on-time, quality data. Document and mai
REGULATORY AND START-UP
Summary of Responsibilities: Draft, review, negotiate, and finalize Clinical Trial Agreements (CTAs), confidentiality agreements, amendments, and related site contract documentation. Coordinate with s
Centralized Study Spec 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 Science Coordinator - II
Job Overview: Assist with the overall Clinical Safety and/or PSS operations associated with products including the adverse events process which may include safety data collected from clinical trials a
Central Monitor I
Job Overview: The Central Monitoring Specialist is responsible for the execution of key Central monitoring (Site, subject and study level review as applicable) activities and in assisting the executio
Safety System Manager, Argus SME
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
Senior Manager, Process Compliance Review and Analysis
Job Overview: It is the responsibility of the post holder to provide all clients, both internal and external, with the appropriate quality of service in a safe and cost-effective manner. The individua
Lead 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
Senior Safety System 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
Centralized Study Specialist I
Summary of Responsibilities: Follow all applicable departmental Standard Operating Procedures and Work Instructions. Complete day-to-day tasks ensuring quality and productivity. Execute high quality,
Study Start-up Associate (Site Activation Specialist)
Job Overview: Primary contact with investigative site(s) during site start-up activities and maintenance with responsibility for collection of the required investigator and essential documents for a s
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
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
Central Monitoring Associate Manager
Job Overview: Responsible for the execution of key central monitoring (site, subject and study level review as applicable) activities. Collaborates within a matrix environment, communicates proactiv
Associate Validator II
Job Overview: Serve as a member of the project team with primary responsibility for all documentation requirements in support of Global EDC Solutions tasks to include receiving and logging-in and scan
Sr Programmer Analyst
Job Description Job Overview: Lead the development and implementation of solutions to global technical services issues and concerns regarding EDC tools like Medidata RAVE or Oracle Inform or Data/Repo
Senior RFI Manager
Summary of Responsibilities: Owns all aspects of the appropriate request for information (RFI) process for assigned opportunities (inclusive of managing opportunities under general supervision, establ
Central Monitor Assistant
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
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