Regulatory Affairs Director

Netherlands  ‐ Vor Ort
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Beschreibung

RE: Regulatory Affairs Director - Immediate Start

I am working with a client of mine who are looking for a Regulatory Affairs Director who has extensive experience working with Oncology Products.

Responsibilities:


  • Facilitate submission approvals and amendments through leading communications (face to face meetings, teleconferences, etc.) and negotiations with clients, government agencies, and project teams.


  • Proactively anticipate and develop initial or alternative regulatory strategies, consulting with other resources within the organisation as required. Provide clients with strategic advice in response to their queries, based on regulatory experience and area of expertise.


  • Responsible for managing work-flow including prioritising project objectives and establishing time frames for projects with clients. Responsible for overseeing progress and completion of projects with project team members, ensuring time frames and deadlines are met.


  • Lead participate in and support project teams and advise other departments on regulatory issues and strategies related to EU filings and maintenance activities across a broad range of product types.


Skills and Experience Required:


  • Science degree is preferable (bachelor's or master's)


  • Experience in supporting business development activities


  • 10+ year's Regulatory Experience


  • Oncology Experience


Apply here if you are interested in this opportunity or if you would like a confidential discussion about your career opportunities please contact Aqil Omr at EPM Scientific.
Start
09/2019
Dauer
6-9
Von
Glocomms
Eingestellt
20.08.2019
Projekt-ID:
1812152
Vertragsart
Freiberuflich
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