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Regulatory Affairs Associate Doc mgmt

Job LocationCambridge
EducationNot Mentioned
Salary200.00 - 350.00 per day
IndustryNot Mentioned
Functional AreaNot Mentioned
Job TypeContract , full-time

Job Description

REGULATORY AFFAIRS ASSOCIATE | VEEVA | DOCUMENT MANAGEMENT | SUBMISSIONS | CONTRACT An innovative biopharmaceutical company are looking for a Regulatory Affairs Associate to join their UK team. They are a top 10 global biopharma company with very exciting portfolios and opportunities for career growth.I am excited to be recruiting for a Regulatory Affairs Associate on an initial 12 month contract. This role is looking for an articulate regulatory operations professional who has a document management and administrative background.The main responsibilities of the role:

  • Working on document management. Tracking regulatory files and systems
  • Interface with Health Authorities
  • Ordering and tracking of regulatory requirements (registration samples, legal documentation, certificates)
  • Planning and preparation of regulatory submissions
Requirements
  • Life Sciences degree
  • Previous experience working with regulatory document management systems (Veeva, Liquent)
  • Previous experience supporting Regulatory submissions
  • minimum of 2 years document management experience in a life sciences background.
This will be a full 12 month contract, with scope for extension. You will need to be on site for 1-2 days in CambridgeWhat you need to do nowIf youre interested in this role, click apply now to forward an up-to-date copy of your CV, or call us now.If this job isnt quite right for you but you are looking for a new position, please contact Julia Bowden for a confidential discussion on your car

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