We're sorry, the job you are looking for at Teva on EuroPharmaJobs has expired.
Click here to see more jobs at Teva .
We still have many live jobs. Click below for similar jobs in:
or go to our job search page.
You will be a contributor to a Global Team with collective responsibility for regulatory activities associated with global pharmacovigilance including electronic pharmacovigilance system, adverse drug experience (ADE) reports, trending reports, ADE
Define and lead the execution of global regulatory CMC strategies for device & combination products to ensure successful approvals in key markets and Compliance throughout development and lifecycle. Performs risk analysis for determination of probability
You will be responsible for defining and implementing the regulatory pathway, from early strategy through to dossier submission, working closely with CMC, Clinical, Medical, and Quality teams. Define and implement the global registration strategy (Main
In this role, the candidate will represent RA in the Clinical Trial Teams and work closely with the CRO and internal stakeholders to ensure regulatory oversight and progress of the clinical trial submissions in EU/ROW. The candidate may also
This key role will be responsible for ensuring the development and delivery of science-based, solution-oriented, and internally aligned regulatory CMC strategies for the program(s) under his/her accountability. Create high quality compliant CMC