Pharmiweb ChannelsAll | PharmaCo | Clinical Research | R&D/BioTech | Sales/Mktg | Healthcare | Recruitment | Pharmacy | Medical Comms

Pharmiweb.com RSS Feed Pharmiweb.com RSS Feeds

Job Details

Drug Safety (Senior) Manager / Lead a Drug Safety Team for EU and International projects – Salary to 90k + Car + Bonus - Gent, Antwerp, Belgium

Company: Advanced S&S (Medical / Clinical)
Location: Gent Area, Belgium
Reference: TMADV / 10340
Closing Date: 14 Mar 18
Type: Full Time
Salary (£): On Application
Benefits: On Application

Top Job

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:

My client is a global Healthcare giant that develops, manufactures, packages and distributes over-the-counter and prescription pharmaceuticals, nutritional products, active pharmaceutical ingredients and consumer products.

They are now expanding their EU and Global Drug Safety Teams in a number of new areas. This particular role reports into a highly regarded QA/PV expert and there are real opportunities for growth, development and frequent promotions. The salary and benefits package are really strong and the role is designed to steadily grow in responsibility and seniority.

As the Drug Safety (Senior) Manager 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.

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 or Pharmacist
  • You have at least 4 years of significant and successful experience in international Drug safety with 2 years in Risk Management Job and/or safety documents writing and signal detection
  • High level proficiency in signal detection and evaluation
  • Previous line management of small teams would be advantageous
  • Experience in medical writing

 

If you have a friend or colleague who you feel may be more suitable please refer them to us, as we offer a new laptop or iPad/tablet for any referrals that we place into a new role…!!!

_____________________________________________________________________________________

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.
_____________________________________________________________________________________

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, Drug Safety, Drug Safety Belgium, PhV, Jobs in PhV, Jobs in Drug Safety.

 

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

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

Advertising
Site Map | Privacy & Security | Cookies | Terms and Conditions

PharmiWeb.com is Europe's leading industry-sponsored portal for the Pharmaceutical sector, providing the latest jobs, news, features and events listings.
The information provided on PharmiWeb.com is designed to support, not replace, the relationship that exists between a patient/site visitor and his/her physician.