When our values align, there's no limit to what we can achieve.
At Parexel, we all share the same goal - to improve the world's health. From
clinical trials to regulatory, consulting, and market access, every clinical
development solution we provide is underpinned by something special - a deep
conviction in what we do.
Each of us, no matter what we do at Parexel, contributes to the development of a
therapy that ultimately will benefit a patient. We take our work personally, we
do it with empathy and we're committed to making a difference.
ABOUT PAREXEL
Parexel is a leading clinical research organization providing comprehensive
services to the pharmaceutical, biotechnology, and medical device industries. We
are committed to advancing clinical research and bringing innovative therapies
to patients worldwide. Our diverse team of professionals is dedicated to
delivering excellence in regulatory affairs, clinical operations, and data
management.
REGULATORY SUBMISSION COORDINATOR – SR ASSOCIATE
ABOUT THE ROLE
Join Parexel's Regulatory Affairs team as a Regulatory Submission
Coordinator and play a critical role in bringing innovative biological products
to patients across Latin America. Reporting to the Regional Submission
Coordinator Lead, you'll be the operational backbone of our regulatory
submission process—coordinating complex documentation, managing timelines, and
ensuring compliance across multiple countries in the LATAM region.
This is an opportunity to work at the heart of regulatory excellence,
collaborating with regional regulatory teams, health authorities, and
cross-functional stakeholders to deliver high-quality submissions that meet the
highest standards.
THE OPPORTUNITY
Sr Associate Level: 4+ years of experience in Regulatory Submissions of
Biological products (mandatory)
It is required to be based in México, Argentina or Brazil (Mandatory)