15 Aug
|
Nexcella
|
Montreal
Nexcella, Inc. is seeking an Associate Director of Regulatory Affairs to guide regulatory strategy and execution for clinical trials under FDA/EMA/Health Canada/MHRA regimes.
The role focuses on preparing, submitting, and maintaining regulatory documents to ensure compliance with applicable laws, with attention to detail and solid analytical skills. Ideal candidates have 3–5 years in regulatory affairs within biopharma and experience with eCTD submissions and regulatory software tools.
📌 Associate Dir, Regulatory Affairs — Clinical Submissions (Montreal)
🏢 Nexcella
📍 Montreal