24 oct
|
Parexel
|
Ciudad de México
24 oct
Parexel
Ciudad de México
Parexel, a integral clinical research partner, seeks a Regulatory Affairs Sr. Associate focused on LATAM COFEPRIS interactions to support product lifecycle management.
You will drive regulatory strategy, oversee submissions, labeling reviews, and post‑approval changes, collaborating with global and regional teams to ensure timely, compliant approvals.
The role requires 5+ years in pharma, strong English and Spanish, and a track record with CTD submissions and regulatory filings across LATAM.
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📌 LATAM Regulatory Strategist - ID & Biologics (Ciudad de México)
🏢 Parexel
📍 Ciudad de México