Since Teva’s establishment in Jerusalem in 1901, our aim has been to help patients live longer, healthier lives. As we work to find solutions to tomorrow’s biggest healthcare challenges, we look back with pride at our humble beginnings and past accomplishments. When, over a century ago, Chaim Salomon, Moshe Levin, and Yitschak Elstein came together in Jerusalem to form a small pharmaceutical business, they could not have imagined that their company would go on to be a world leader in the industry.
Vacancy Details
If you’re a Science Graduate/Post Graduate having below:
• Experience in Startup, Conduct & Close out activity. (End to end into clinical data management)
• Experience in any EDC tools i.e. RAVE/Medidata RAVE, Veeva.
• 3-6 years of experience.
The incumbent will be responsible for:
• Review study protocol and case report form.
• Performing data management activities like query management which include query generation & query resolution.
• Perform SAE reconciliation and Lab/Vendor data reconciliation.
• Preparation & review of:
– DVS (Data Validation Specification)
– Manual listings for the study.
– eCRF Completion guidelines for the study.
– Time & Event schedule for the study.
– UAT (User Acceptance Test)
Drive Date – 20th Dec’22 ( Tuesday )
Please reach out to me in my email address poulomi.mitra@teva.co.in mentioning ( Interested for CDM drive)
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