Regulatory Affairs Senior Specialist

Job Description

927 million. The number of lives we touched in 2017. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this how can we continue to improve and extend even more people’s lives

We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks. And where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges.

We are Novartis. Join us and help us reimagine medicine.

Job purpose
Our team covers the RA needs for the entire Novartis Group in Romania.
We are currently looking for a new colleague to join the team and perform all activities associated with obtaining and maintaining marketing authorizations for assigned pharmaceutical products. The person will also be in charge with monitoring renewals, post-authorization variations, registering clinical trials, monitoring the process of clinical trial registration, and applying for amendments to ongoing clinical trials.

Minimum Requirements

• University degree in Pharmacy, Medicine, Biology, Chemistry;
• Fluent written and verbal English;
• At least 3-4 years in RA similar positions;
• People management experience is a plus.
  

Division
Global Drug Development
Business Unit
REG AFFAIRS GDD
Country
Romania
Work Location
Bucharest

Company/Legal Entity

NOV PHA SERVICES ROU
Functional Area
Research & Development
Job Type
Full Time
Employment Type
Regular