Pharmacovigilance Officer – EU role with training and great development opportunities!

Ghent, Belgium
On Application
10 Oct 2019
09 Nov 2019
TM/310719 R4
Theo Moore
Full Time
Contract Type
Experience Level
Experienced (non-manager)

Pharmacovigilance Officer – Join a growing organization, in a role that comes with training and development opportunities!

Location: Based close to Ghent but with options to work a few days a week from home, so commutable from Brussels, Antwerp and Bruges.

My client is growing and expanding and is already acknowledged as one of the largest and most dynamic companies in the Pharmaceutical, consumer health and personal care industry, with a huge number of Global International brands. They are rapidly expanding and constantly looking for dynamic people who are looking for real career opportunities.

They are offering the right candidate a hugely exciting, rewarding and challenging opportunity, working with a highly regarded Head of Quality and PV.

The culture here is easy to describe, it’s one of innovation and is focused on teams having what they need to be able to deliver in a customer focused organisation.  This will be a key position in a growing organization in a dynamic, rapidly expanding   multinational company environment.

The perfect candidate will have a 1 to 4 years Pharmacovigilance experience and be looking for a role that that will lead to further opportunities.

You will work within a dynamic European PV team to cover a wide variety of PV activities including:

  • You discuss the content and strategy of safety documents with important stakeholders within the Benefit/Risk Group and Global Regulatory
  • You participate on writing responses or contributions for the health authorities related safety enquiries.
  • You work with a cross functional team to realize deadlines for health authority requests and submissions.
  • Ensure that safety documents (e.g. periodic reports, signal evaluations, regulatory enquiries, risk management plans) are written accurately and in a timely manner to meet global compliance and regulatory
  • Provide support for submission of PSUR’s
  • Assist in creations of core structured benefit-risk assessments, core Risk Management Plans (RMPs), and EU

The salary and package are very competitive, and you would expect from a global market leader, and you the you will receive a strong and competitive benefits package.

To learn more and apply for this role, please send your CV with a covering note to can also contact. me, Theo Moore on +44 (0)207 801 3384 or +44 (0)7918 195 166 for an initial discussion about the role and other projects.

About Advanced Search & Our Network

Advanced Search, has a network of affiliated companies including ADV Regulatory, and ADV Talent Partners. Together, we are specialists in Regulatory Affairs and Life Sciences recruitment especially around mAbs and biologicals for roles in R&D and Commercialization and have been established and hiring in this area since 2005.

Our team know our subject matter areas and our mission is to help you grow your career each and every step of the way. We have helped many of today's leading companies develop strong regulatory sciences functions and are known for hiring complimentary teams that work well with each other, at owner-contributor, strategy leading and people management levels.

We provide a high level of service because we believe this matters.

Contact us today to see how we can help you, make that next career move on

+44 (0)20 7801 3380

All applications are kept in confidence and we invite applications from all members of the Academic, Research & Development based bio-/pharmaceutical community.

Keywords / Key words: Pharmacovigilance Officer / PV / PV Offices, Healthcare Officer, Healthcare Project Manager, Quality and PV Manager

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