Sr Director Of Regulatory Affairs

San Diego  ‐ Onsite
This project has been archived and is not accepting more applications.
Browse open projects on our job board.

Keywords

Description

Seeking an ambitious and talented candidate in Regulatory Affairs to lead a small and well-funded orphan drug company. The right individual will have the opportunity to take on initiative and work cross-functionally with high-level executives to achieve and implement regulatory intelligence and strategy. If you are ready to work among some of the most well-known individuals in regulatory affairs, and meet the requirements below please reach out.

Requirements:

- 7-10 years of global regulatory lead experience at a pharmaceutical/biotech company

- led and filed NDA submission

- Strong knowledge of FDA & EMA regulations

- Conducted and led cross-functional teams

- Direct interaction with FDA

- Experience building a team/new department in regulatory affairs

- Experience filing abroad

- Management experience, or experience building regulatory teams

If you are ready to set yourself apart from big pharma and build your career, please forward an updated resume to the information below.
Start date
07/2014
From
Real Staffing
Published at
05.07.2014
Project ID:
737186
Contract type
Permanent
To apply to this project you must log in.
Register