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Regulatory RIMS Specialist

  1. France
Paris
  1. Contract
Competitive
  1. Drug Safety / Pharmacovigilance
32219
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Regulatory RIMS Specialist - Life Science - 6-Month Contract - France/UK 

This is a unique opportunity for a Regulatory RIMS Specialist to join our client – an esteemed partner for regulatory and compliance in healthcare. This is a contract opportunity of at least 6 months within the stunning city of Paris/London. With a globally established presence spanning over 140 countries and partner to some of the top pharmaceutical companies, this is a fantastic company to join to progress your career.


Responsibilities 
  • Supporting Regulatory Affairs Officers in their routine use of Veeva RIM
  • Carry out activities with them in RIM, or for them in RIM
  • Suggest improvements in use, on a specific case or on processes in general
 
Requirements 
  • Experience as a Regulatory Affairs Officer
  • Good knowledge of regulatory processes and issues as a whole
  • Advanced contribution to projects, project management
  • Animation of community / communication

If this role is of interest to you, please apply now! 

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