Role Activities

• Prepare dossiers
• Coordinate documentation
• Manage records

Requirements Summary

5–10 years regulatory dossier experience for international markets; MENA registrations; proficient with Veeva Vault RIM; strong knowledge outside EU/US; bachelor's in Life Sciences, Pharmacy, Regulatory Affairs; excellent organization and cross-functional collaboration.

Other Requirements

BridgeBio Pharma

<p><strong>BridgeBio</strong> is a biopharmaceutical company founded to discover, create, test, and deliver transformative medicines to treat patients who suffer from genetic diseases and cancers with clear genetic drivers. We bridge the gap between remarkable advancements in genetic science in academic institutions and the delivery of meaningful medicines to patients. Founded in 2015, the company has built a portfolio of 20+ drug development programs ranging from preclinical to late-stage development in multiple therapeutic areas including genetic dermatology, precision oncology, cardiology, endocrinology, neurology, pulmonology, and renal disease, with two approved drugs. <br><br>Our focus on scientific excellence and rapid execution aim to translate today’s discoveries into tomorrow’s medicines. We have U.S. offices in San Francisco, Palo Alto, and Raleigh, with small satellites in other parts of the country. We also have international offices in Montreal, Canada, and Zurich, Switzerland, and are expanding across Europe. <br><br>To learn more about our story and company culture, visit us at <a href="https://bridgebio.com"><u>https://bridgebio.com</u></a></p>