Full-time
CSR Documentation Specialist & eTMF Editor
Posted by IQVIA LLC • Mexico, ciudad de méxico, Mexico
About the Role
IQVIA LLC in Mexico City is seeking a Clinical Document Specialist to manage the creation and quality control of Clinical Study Report appendices. The role involves leading timelines and coordinating essential documents in compliance with regulatory requirements.
The ideal candidate should have a Bachelor’s degree in a relevant field and at least 1-2 years of eTMF experience. Strong fluency in English and attention to detail are essential for success in this fast-paced environment.
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