Pharmacovigilance Expert - Den Bosch

Vacancy information

Publication date:June 03 2020
Employment type:Permanent
Sector:Clinical Research
Function Group:Pharmacovigilance

Function Group: Pharmacovigilance / Pharmacovigilance

Organization

For the office in the Netherlands based in Den Bosch, we are looking for a Pharmacovigilance Expert with several years of experience. Operating around the Benelux with offices in Den Bosch, this topnotch consultancy firm provides clients with a wide variety of global support. This consultancy firm is in the top three most promising privately owned consultancy companies in the Netherlands. The office based in Den Bosch with 30 colleagues, is serving its clients with an initial clinical study to post-approval compliance. They are working especially for chemical and biological medicinal products and medical devices. Since they are working together with the local people, they are very successful in deeply rooted relationships with clients by providing leading industry knowledge, experience, and proven processes. This mid-size company has close to 30 clients worldwide, 35+ colleagues from Pharmacovigilance, RA managers to CMC experts, and is supporting her clients in whole Benelux.

Function

Are you interested in an independent, responsible and consulting role in a small consultancy firm with possibilities to (further) develop yourself as a Pharmacovigilance Expert? You will work for several clients on projects with a duration between six months and three years. Because the work-life balance is really important for the employees of this company, everybody will take care that you will work on a project that you like and are close to home. You will be working for state of the art pharma companies and little local start-up’s. You will help those companies with a very wide variety of services, such as review reports on pharmaceutical product and process development, prepare and coordinate submissions and authorization procedures and “translate” scientific lab results into drug safety supportive dossier documents. In this role, it is important that you are able to have effective communications with clients and that you can work autonomously on projects. It goes without saying that you have over twenty-five colleagues that will have your back and support you. Because when you are working at a client, the client actually hires the knowledge of over twenty-five international consultants.

Requirements

The ideal candidate has:

  • Preferably, a PhD in Pharmacy, Medical Biology, Life Sciences
  • Minimal 5 years of experience in the pharmaceutical industry and PV
  • Knowledge of pharmacovigilance, pharmacovigilance systems and GVP modules
  • The ability to handle deadlines and changing priorities in a dynamic environment
  • The ability to communicate effectively based on scientific knowledge
  • The will to live up to the Zwiers “professional approach with a personal touch” spirit

Offer

In exchange for your talent, time and energy we offer:

  • Salary midpoint around €60,000 depending on experience
  • Pension scheme
  • Holiday allowance
  • Work in an international environment of pharmaceutical industry
  • Interesting projects which will stimulate you to keep learning
  • Company car

Application

If you are interested in this job, or in similar ones, please feel free to contact me directly.

Yvo Selderbeek
Senior Associate – Clinical Research

+31(0)6-12576648
+31(0)23-7548660
y.selderbeek@qtcrecruitment.com

Apply

Contact

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