Pharmacovigilance / drug safety professionals (juniors and experts)

We are continuously looking for experienced pharmacovigilance professionals to reinforce our Valesta team.

  • You are fluent in English?
  • You have experience with safety and regulatory data?
  • You see report writing as a daily part of your job?

Then you might be the Pharmacovigilance professional we are looking for!

Responsibilities 
  • Reviewing, assessing and processing safety data for phase I, II & III clinical trials and marketed products
  • Maintaining information about all SAEs/ADRs in a secure location, in accordance with local regulations
  • Tracking of regulatory guidelines and directives related to Medical Affairs department activities
  • Maintaining a ‘list of Authorities and other official bodies’ to whom SAEs/ADRs should be reported, as well as corresponding reporting procedures
  • Review of listings, concomitant therapy, line listings, clinical trial protocols, …
  • Report writing: narratives, DSURs, PSURs, product related expert reports, ISSs, Clinical Expert Statements/Clinical overviews for registration reneweal purpose, involvement in writing of the safety section of the IB, SDEA, SPP,…
  • Direct reports, backup and internal/external communication
Profile 
  • You are a Medical doctor, Pharmacist, PhD or equivalent by experience
  • Experience within pharmacovigilance is preferred
  • You are fluent in English, knowledge of French or Dutch is an asset
  • You have excellent organisational skills
  • You show strong planning skills and easily respect timelines
  • You are a flexible team player, highly rating confidentiality
  • You are very punctual and accurate in your work
Contact Information 

Nele Daems
nele.daems@valesta.com
015 21 11 04

Application form : Pharmacovigilance / drug safety professionals (juniors and experts)

Files must be less than 3 MB.
Allowed file types: txt rtf html pdf doc docx odt.
Files must be less than 3 MB.
Allowed file types: txt rtf html pdf doc docx odt.

I want to stay informed.

I would like to receive Valesta news, valuable insights into industry trends, career opportunities, trainings, and other helpful tips to find assignments that match my skills and interests. Click here to stay connected with Valesta.

Valesta is an expert in life science recruiting and project staffing.  The information you are submitting is important for us to respond to your assignment and contract needs. In compliance with the General Data Protection Regulation (EU) 2016/679) (“GDPR”), Valesta will process your personal data in accordance with our Privacy Policy. Valesta will safeguard your personal information and not disclose to any person unlawfully. As a staffing company, Valesta receives and processes your personal data for the following purpose: to take appropriate steps to find you an assignment with one of our clients and/or to finalise a contract with you.

Please note that Valesta does not wish to receive any data from you if you are under the age of eighteen (18) or data that is classified as Sensitive Data under the GDPR; this includes personal data revealing racial or ethnic origin, political opinions, religious or philosophical beliefs, trade union membership, genetic/biometric/health-related data or data concerning a person's sex life/sexual orientation.

Please read our disclaimer.