Junior Regulatory Affairs Administrator

To meet the upcoming demand of several of our clients in the Pharmaceutical Sector, we are looking for Junior Regulatory Affairs Administrators.

  • Do you have a University Degree related to Life Sciences?
  • Do you have a first experience in Regulatory Affairs or did you accomplish an additional training, specifically in Regulatory Affairs (+ internship)
  • Are you fluent in English?

Then you might be the candidate we are looking for. Don’t hesitate and apply now!

Job Description 

As a Regulatory Affairs Administrator, you work within the Regulatory Affairs Unit. 

 

Responsibilities 
  • You prepare, handle, distribute and file submissions to national Competent Authorities, Central/Local Ethics committees throughout the European continent.
  • You work according to standard operating procedures, European Directives and applicable country legislation
  • You develop expertise in assigned territories and general clinical trial environment.
  • You contribute to building and improving internal processes
  • You are responsible for document management, including maintenance of working paper and electronic files and tracking of regulatory documentation within the E-TMF
  • You interact with the internal clinical teams, regulators and scientific network

Responsibilities and career opportunities are adapted depending on the candidate's skills.

Profile 
  • You have a university degree in life sciences
  • You have an experience in Regulatory Affairs related to clinical trials environment (CRO or university/ hospital or pharmaceutical industry) or, you accomplished an additional training, specifically in Regulatory Affairs (+ internship)
  • You are proficient in English (oral and written), any other language is an asset.
  • You are proficient in Word, Excel & PowerPoint, skills in SharePoint are an asset
  • You have the ability to cope with and meet tight timelines when required.
  • You are able to manage multiple tasks at the same time
  • You are able to work independently as well as part of a team
  • You have strong organization, time-management and communication skills
  • You have an excellent attention to details
Important 

Amandine Planche
+32 10 68 53 30
amandine.planche@valesta.com

Application form : Junior Regulatory Affairs Administrator

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.