Teva Pharmaceuticals Released Job Openings On 23/05/2022.Teva is a global pharmaceutical leader and the world’s largest generic medicines producer, committed to improving health and increasing access to quality health solutions worldwide.Application form link provided at the end of post.
Vacancy Details:
Teva Pharmaceuticals Recruiting Any Graduate with 4+ years of Experience for Clinical Data Management Lead Position.Complete Details for the Clinical Data Management Lead as follows.
Important Details :
- Location : Bangalore/Bengaluru( Hebbal )
- No of Vacancies:01
- Details of Salary:₹ 10,00,000 – 15,00,000 P.A.
- Opening date for online Application: 23/05/2022
- Mode of application :Online
- How To Apply: At the End of the Article We Have Provided Source Link,Please Go through that and Follow Necessary Steps
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Job Description/Skills Required
- 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.
- Preparation and review of Time and Event schedule for the study.
- Creation and review of UAT (User Acceptance Testing).
- Performing UAT (User Acceptance Testing) of the edit checks for the study.
- Performing Data Management activities like query management which include, query generation and query resolution.
- Perform SAE reconciliation and Lab/Vendor data reconciliation.
- Generating metric reports/ status reports for the DM status for the study and updating it to assistant manager CDM.
- Perform Dataset review at the time of Database lock.
- Freeze and lock the data as appropriate in time for the statistical analysis.
- Documenting of the DM activities/tasks for the project.
- Updating study status and informing any study related issues to the Assistant Manager/Deputy Manager/Manager/Senior Manager CDM when required for the further action.
- 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.
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