We are growing, grow with us!

Are you eager to work in a dynamic company where new challenges and opportunities are part of your every day life? Then make PharmaLex your career choice!

PharmaLex is the leading service provider for the worldwide pharmaceutical industry in regulatory affairs, pharmacovigilance and development consulting. 
We are specialized in effectively designing all aspects of drug and medicinal product registrations - ranging from early development and market entry to product maintenance activities.

In Denmark we are looking for a Senior Pharmacovigilance Specialist with a strong pharma background.

Senior Pharmacovigilance Specialist

Your responsibilities

As a part of our Pharmacovigilance team, your responsibilities will include, but not be limited to, the following:
  • Participate in pre- and post-market drug safety projects in a global organization
  • Management of adverse drug reactions
  • Production and review of periodic safety re-ports and risk management plans
  • Literature search
  • Safety reporting to competent authorities
  • Set-up and maintain global pharmacovigilance systems

Your profile

  • Academic degree in pharmacy or life science
  • At least 5 years of experience in Pharmacovigilance
  • Well organized and sense of accuracy
  • Flexible and committed to meeting deadlines
  • Fluency in spoken and written English

We offer you

Exciting and varied challenges in a friendly team, as well as many opportunities for personal development and job training.


For further information please contact:
Cecilia Falkenberg, Senior Director Regulatory Affairs & Pharmacovigilance
Phone: +45 78 79 95 14, Mobile: +45 51 64 91 50

If you are interested in taking on this challenging job opportunity in our future-oriented company, we are looking forward to receive your application online. Please apply as soon as possible since work with recruitment is being done on a continual basis.

To apply, please use the "apply now" button below.