R&D
Intern Teva Pharmaceuticals M.Sc. in any life sciences/M.Pharma/ B.Pharma/ B.Sc./ B.Tech Biotechnology
Job
Description
Review
Study protocol and Case Report Forms.
Preparation
and review of DVS (Data Validation specification).
Preparation
and review of manual listings for the study.
Preparation
and review of eCRF Completion guidelines for the study.
Performing
UAT (User Acceptance Testing) of the edit checks for the study.
Performing
DM activities like query management which include, query generation and query
resolution.
Perform
SAE reconciliation and Lab/Vendor data reconciliation.
Updating
study status and informing any study related issues to the Assistant Manager
Prioritize
and plan the tasks efficiently to meet the project deliverables in time.
Developing
eCRF using Clinical Data Management systems.
Programming
edit checks and deploys study to production.
Performing
post production changes and assessment of impact on database.
To
carry out other responsibilities and as when assigned by the management.
Qualifications
M.Sc.
in any life sciences/M.Pharma/ B.Pharma/
B.Sc./ B.Tech Biotechnology
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