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Job Details

Drug Safety MD - Associate Director & Team Leader (for 5 FTE's) - Lead the benefit risk evaluation unit - Belgium

Company: Advanced S&S (Medical / Clinical)
Location: Belgium - with options to be home based
Reference: TMADV / 191118C
Closing Date: 19 Dec 18
Type: Full Time
Salary (£): Negotiable
Benefits: On Appplication

Job Summary:

If you wish 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.

Requirements:

Drug Safety MD - Associate Director & Team Leader (for 5FTE's) -  oversight on the signal management process - Great Salary + Car + Bonus!

Location: Based in Brussels at the EU HQ 

We have a new expansive role with a leading pharmaceutical company that has a strong reputation for quality, innovation and staff development where you will  have a full oversight on the signal management process and you will have a key role on the continuous improvement of that process.

As the Associate Director you will lead the benefit risk evaluation unit, supervising the review of Safety reports such as PBRER, RMP, ACO and other related safety documents with a full oversight on the signal management process, playing a key role on the continuous improvement of that process.

This will be an EMEA role with input into Global projects plans and you will manage and supervise the work of external vendors performing the literature search and safety writing and ensuring appropriate KPIs are implemented where appropriate. You will lead a growing team helping to develop the PV function with this successful Global organisation.

Role:

  • Full oversight on the signal management process and you will have a key role on the continuous improvement of that process
  • Co-responsible for the preparation work in relation to signal detection, triage.
  • Co-lead signal management process with other relevant functions (QPPV, medical review)
  • Develop risk management strategies and plans and monitor effectiveness
  • manage & coordinate cumulative safety planning in accordance with timelines as mentioned into signal management procedure
  • Ensure appropriate KPIs are implemented where appropriate.

Experience needed:

  • MD qualification with at least 5 years of significant and successful experience in international Drug Safety with experience in risk management and and signal detection.
  • High level proficiency in signal detection and evaluation and previous line management of small teams would be advantageous (but not essential).

Package:

  • The role comes with a six-figure basic salary, bonus and fully expensed car and high level benefits package with a  home working contract available, but its necessary to be on-site at least 2-3 times  a week.

If you wish 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.

If you wish 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 Search and Selection - Clinical and Medical Division has been operating since 2004. We are registered and licensed to recruit in the UK, Switzerland, Mainland Europe and the Americas - we have offices in both the UK and Switzerland. We are a recruitment business dedicated to the pharmaceutical industry, specialising in Regulatory, Clinical and Medical Affairs.

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

If you wish to apply for this role please click Apply Now, or send your CV with a covering note to CV@AdvRegulatory.com. Alternatively to have a confidential discussion about this or other potential roles or career options, call Theo Moore or Matt Greig in the UK London office, on +44 (0)20 7801 3380.

Keywords / Key words: Pharmacovigilance Associate Director, Drug Safety, Pharmacovigilance Associate Director, Drug Safety, Pharmacovigilance Associate Director, Drug Safety Physician

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

Contact Information:

Address:  Head Office
Head Office Suite 8 Penhurst House 352-356 Battersea Park Road London
SW11 3BY
England
Tel:  +44 (0)20 7801 3388
Website:  Visit Our Web Site

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