We are a large clinical research organization, and we are looking for professional translators who can assist with our Regulatory Affairs Projects.
REQUIRED SKILLS AND EXPERIENCE
Native in target language
Fluency in source language(s) – spoken and written
At least 1 year of experience in translating, reviewing, and/or post-editing regulatory content (SmPCs, CTD, labelling, packaging, etc.)
Experience with translation management systems and CAT tools (memoQ preferred), as well as proficiency in Excel & Word
Freelance (no agencies)
If you’re interested and meet our mandatory requirements, PLEASE APPLY via the below link: https://iqvia.iqvia.teamtailor-enterprise.com/jobs/252-join-our-regulatory-affairs-team
PLEASE NOTE THAT AGENCIES APPLICATIONS WILL NOT BE CONSIDERED.
Thank you!
Ana Martínez | IQVIA Vendor Management
