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Job Details

Regulatory “Tracking Specialist” – The Netherlands - Global Pharma Company – Excellent Rate

Company: Advanced Regulatory (UK & Europe)
Location: Amsterdam and The Hague
Reference: TMADV / 141116C
Closing Date: 14 Dec 16
Type: Full Time
Salary (£): On Application
Benefits: On Application

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Job Summary:

We have a new Regulatory Affairs “Tracking Specialist” role for a yearlong contract with a high probability of an extension for a Global Pharmaceutical company with a dynamic, innovative and entrepreneurial approach to drug development and product registrations. Please call Theo Moore or Matt Greig in the London office on +44 (0)20 7801 3380.

Requirements:

Regulatory “Tracking Specialist” – The Netherlands - Global Pharma Company – Excellent Rate -

We have a new Regulatory Affairs “Tracking Specialist” role for a yearlong contract with a high probability of an extension for a Global Pharmaceutical company with a dynamic, innovative and entrepreneurial approach to drug development and product registrations.

You will be working on a large variety or projects in different stages of development, for different projects across all therapy areas and the hourly rate is very good and will be based on experience, expertise and ability to work independently as well as within a Global team.

This will be at the EU Headquarters based in The Netherlands with options available to work a few days from home.

Major Accountabilities and Responsibilities:

  • Running and disseminating reports on data collected into the global license tracking database.
  • Providing first-line business support and end-user training for use of the global license tracking database. End Users include Global Regulatory Affairs, Technical Operations, Drug Safety, Affiliates and Strategic Partners
  • Submit Product Information directly or indirectly to Health Authorities as required e.g. XVEMPD, PSUR, PSMF
  • Work to specific protocols and procedures for all aspects of data management work
  • Contributing to design/development of new/revised procedures

Experience needed:

  • 3+ years of experience in the pharmaceutical industry, with specific experience related to the processing of regulatory information management.
  • Please contact me for a confidential discussion on the role, company, job specification and possible opportunities for future development.
  • If these roles are not for you but you do have colleagues past or present who are looking please consider referring the individual to us, we do offer an iPad 3 referral scheme on successful placement

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To apply for this role, please send your CV with a covering note to cv@advregulatory.com or alternatively, to have a confidential discussion about this or other potential roles or career options, call Theo Moore or Matt Greig in the London office on +44 (0)20 7801 3380.

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About Advanced

Advanced Regulatory is a division of Advanced Search and Selection Ltd and has been operating since 2004. We are registered and licensed to recruit through the United Kingdom, mainland Europe and the Americas - we have offices both in the UK and in Switzerland. We are a recruitment business dedicated to the pharmaceutical industry, specialising in Regulatory Affairs.

We match professional candidates to the best permanent, contract and interim roles in the market. For more information about the company visit us at www.advregulatory.com.

We provide a high level of service because we believe this matters. Regulatory professionals will find we know our recruitment subject matter.

Keywords / Key words: Regulatory, Regulatory Affairs, Reg Affairs, RA, Regulatory jobs, RA jobs, Regulatory Affairs Jobs, Publishing, Tracking,  Regulatory, Regulatory Affairs, Reg Affairs, RA, Regulatory jobs, RA jobs, Regulatory Affairs Jobs, Publishing, Tracking

To Apply : Please send a full CV in confidence to cv@advregulatory.com.

Contact Information:

Address:  Head Office
Suite 8 Penhurst House 352-356 Battersea Park Road London
SW11 3BY
England
Tel:  +44 (0)20 7801 3380
Fax:  +44 (0)20 7228 1188
Website:  Visit Our Web Site

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