Share this Job

Database Admin Professional II

Date: Jun 19, 2022

Location: Bangalore, IN, 560052

Company: Teva Pharmaceuticals

Company Info

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. Our employees are at the core of our success, with colleagues in over 80 countries delivering the world's largest medicine cabinet to 200 million people every day. We offer a uniquely diverse portfolio of products and solutions for patients and we've built a promising pipeline centered around our core therapeutic areas.  We are continually developing patient-centric solutions and significantly growing both our generic and specialty medicines business through investment in research and development, marketing, business development and innovation. This is how we improve health and enable people to live better, healthier lives. Join us on our journey of growth!

Job Description

  • Overall responsibility to carry the studies from Start-up to close-out.
  • Checking the team's quality deliverables and providing the quality metric to the reporting managers for continuous improvements.
  • Collaboration with cross geographical stakeholders and providing the inputs regarding the CDM activities carried out for the study assigned.
  • Assisting the team members in providing the automation ideas for smooth transistion of work.
  • Review of the Study Protocol and Case Report Forms
  • Preparation and Review of Data Validation Specification (DVS).
  • Preparation and review of manual listing of the study, eCRF Completion guidelines,DMP
  • Create and review of the test scripts for the UAT (User Acceptance Testing)
  • Performing UAT of the edit checks and screens review of the study.
  • Performing the Data Management activities of the studies like query management which includes query generation and query resolution.
  • Performing external data reconciliations (SAE and Lab data).
  • Generating metric reports/study status reports for the DM status of the study and updating the stakeholders of the study.
  • Documentation of the study activities as per SOP and regulatory guidelines.
  • Freezing and Locking of the database.
  • Performing the Post production changes and assessing the impact for the changes.

Qualifications

M.Sc/ M.Pharm

Function

Information Technology

Sub Function

Database Administration

Already Working @TEVA?

If you are a current Teva employee, please apply using the internal career site available on "Employee Central". By doing so, your application will be treated with priority. You will also be able to see opportunities that are open exclusively to Teva employees. Use the following link to search and apply: Internal Career Site

The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner.

Teva’s Equal Employment Opportunity Commitment

Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws.