Join AbCellera as a Clinical Study Start-Up Manager and manage start-up projects for groundbreaking clinical trials. Ensure high-quality document handling and regulatory compliance in an accelerated environment.In this critical role, you'll lead the start-up activities through hands-on management of document collection and regulatory submissions. Your expertise will help streamline the selection and qualification of study sites, ensuring adherence to global regulatory standards. Your efforts in resolving contract negotiations will further enhance study timelines.Key Responsibilities:Manage document collection and rigour for site activationCollaborate on submission packages with Regulatory teamMaintain Trial Master File in inspection-ready conditionSupport site qualification and feasibility assessmentsAddress queries from health authorities promptlyRequirements:Bachelor's degree in Life Sciences or similar8+ years of related clinical research experienceDirect experience in start-up and site activationFamiliarity with Canadian clinical trial regulationsStrong organizational and communication skills, bilingual preferredYour proactive involvement will be key to delivering creative therapies to those in need.

📌 Lead Clinical Trial Start-Up Projects (Montreal)
🏢 AbCellera
📍 Montreal