This site uses cookies. By continuing to browse the site you are agreeing to our use of cookies. Find out more here.

Close Message
NextPharmaJob.com for pharmaceutical industry jobs
Pharma-Search Ltd
NextPharmaJob.com is dedicated to putting job seekers looking for pharmaceutical industry jobs in touch with recruiters and employers.

Similar jobs you may be interested in:

Change Control Systems Manager- International Project
UK - South East
Associate Director of Regulatory Affairs - Labelling - Pharma
UK - South East
Regulatory Affairs Advisor
United Kingdom
Regulatory Affairs Associate -Full relocation package on offer!
United Kingdom
Regulatory Director, Strategic Role, Pharma/Medical devices
Switzerland
More...

To receive a FREE weekly email alert of all the latest pharmaceutical industry jobs added to our database enter your email address below.

Submit | Tell me more...

Sister site:
Our sister site
Job Details
This job has expired. Click here to view similar jobs.

Vice President Scientific Affairs and Regulatory Engagement, Switzerland



Business Type: Pharmaceutical Company
Job Type: Regulatory Affairs, Other Business Support
Job Level: Not Specified
Position: Full Time
Salary: Attractive Salary Package Commensurate with experience
Location: Switzerland
Reference: PSL4021
Background:
Join a highly successful business and market leader to help continue the growth of their focused and ambitious product development pipeline.

Reporting to the Senior Vice President Research & Development you will play a crucial role in the strategic leadership and direction for the scientific integrity of all regulatory submissions and approvals.
You will be a key member of the senior executive leadership team within R&D, accountable for the scientific quality of product submission dossiers, and their successful approval by regulatory authorities.

Under your guidance and scientific leadership, you will be responsible for managing:
  • Council of Fellows
  • Scientific Advisory Board (external)
  • Scientific Engagement
  • Quality Management
You will have full responsibility for the scientific content of future regulatory submissions, ensuring that all research and data are of the highest quality standards.

You will have a high level of autonomy, decision making responsibility and be expected to possess excellent communication and management skills in order to develop outstanding relationships with internal and external stakeholders and regulatory agencies.

Crucial to your success will be your ability to work closely with the FDA and other regulatory bodies to agree innovative scientific approaches and provide the internal leadership to convert this into a regulatory strategy to be followed and implemented.

Scientific standards will be established through a Quality by Design approach to all aspects of the research, including non-clinical and clinical assessment, behavioural studies, manufacture and post marketing surveillance.

Ideally you will have an innovative and pragmatic approach, a desire to make a difference and the ability to lead and motivate others through your passion and enthusiasm. Your communication skills will allow you to interact at all levels, share complex information and work closely with the executive leadership team and Board. You will provide scientific and regulatory leadership and ensure full compliance whilst appreciating when to consider a more creative and pragmatic approach whilst ensuring scientific integrity and robust data.

This is an exciting opportunity to join a highly successful global business, within a leadership capacity, in a highly visible capacity where the long term career prospects are varied and exceptional.

For further information or a discussion in complete confidence, please contact Dr Grant Coren, Pharma-Search Ltd - grant@pharma-search.co.uk, telephone: + 44 (0) 1442 345 340.


Posted: 27/07/2012 | NPJ Ref: 84448
line graphic

Compatible with:

JobMate   Broadbean

Site optimised for Internet Explorer 8+ / Firefox 3+
View a complete Jobs Listing



Credit cards image