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Documentation Specialist

  1. France
Paris
  1. Permanent
Competitive
  1. Drug Safety / Pharmacovigilance
02-06-2023
31189

This vacancy has now expired

Documentation Specialist – Life Sciences – Paris – Permanent

This is a unique opportunity for a Documentation 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. 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.

Documentation Specialist Responsibilities:
  • Implement a document management system for Clinical Studies and contribute to the implementation of an electronic document management system at the global level by being responsible for its compliance in case of inspection
  • Implement the methodology of control and follow-up of the master file of the Clinical Studies
  • Supervise the follow-up of the collection and management of key documents and files by the assistants
  • Ensure the up-to-date filing of documents related to the studies by collaborating with the different contributors (internal and external)
  • Supervise the reconciliation of different types of documents (paper or electronic) throughout the studies
  • Select and implement tracking tools for the different activities and share them with the project teams
  • Train and transmit to the whole clinical department a spirit of management of originator files, in order to be better prepared for audits and inspections
About you:
  • Relevant degree
  • Previous experience within a similar role
  • Pharmaceutical experience.
Are you a good fit for this Documentation Specialist position? Get in touch with us today.

The candidate must have the rights to work in the location stated in the job advert.

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