AbCellera is seeking a meticulous Regulatory Submissions Specialist to lead electronic publishing of clinical development submissions. You will format, compile, and ensure compliance across global health authorities, coordinating with internal stakeholders to meet tight timelines.
You’ll apply 5+ years in regulatory operations, a Bachelor’s degree, and robust experience with eCTD, Veeva RIM, submission gateways, and regulatory processes to ensure high-quality submissions and seamless lifecycle
📌 Global Regulatory Submissions Lead — eCTD & Publishing (Vancouver)
🏢 AbCellera
📍 Vancouver
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