344782BR
May 16, 2022
Russian Fed.

Job Description

Our global portfolio of innovative patented medicines includes more than 50 products, many of which are among the leaders in their therapeutic areas. In Medical Affairs we are encouraged to collaborate grow, and work on new ways to increase our impact in the community.


Your responsibilities include, but not limited:

•Managing a team of regulatory specialist.
•Directs the development of submission of product registration, progress reports, supplements, amendments, and/or periodic experience reports.
•Provides strategic product direction to teams on interaction and negotiates evidence with regulatory agencies.
•Serves as a regulatory liaison on the project team throughout the product lifecycle.
•Ensures rapid and timely approval on of new drugs, biologics/biotechnology and continued approved status of marketed drugs or medical devices.

Diversity & Inclusion / EEO

Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.

Minimum Requirements

You would be a good match for this role, if you have:

• Experience working in a cross-functional matrix structure;
• Strong project management skills;
• Minimum 5 years in regulatory affairs ( as sr specialist or regulatory management);
• English - upper-intermediate.

What we offer for you:

Competitive salary and annual bonus level
Medical insurance (for the employee and children, additional discount given for close relatives)
Life insurance, meal allowance, mobile compensation;
Flexible working hours;
Internal and external educational courses and trainings;
Additional 3 additional days of paid vacation;
Professional and career development opportunities (locally as well as worldwide).

Why consider Novartis?

766 million. That’s how many lives our products touched. 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 reimagine medicine.
SANDOZ
COMMERCIAL OPS EUROPE SZ
Russian Fed.
Moscow
Research & Development
Full Time
Regular
No
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344782BR

DRA Group Head LCM

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