Take the lead in clinical research as a Clinical Study Start-Up Manager at AbCellera. Oversee start-up processes to accelerate creative medicine development efficiently. At AbCellera, you will be the driving force in managing critical start-up activities for clinical trials.

Your extensive background in document oversight, regulatory submissions, and site activation will ensure compliance and efficiency. Work closely with internal teams and site staff to facilitate negotiations and manage timelines effectively throughout the study activation phase. Key Responsibilities:

- Coordinate essential site document collection and review
- Ensure regulatory submission timelines are met
- Facilitate CTAs and budget negotiations with stakeholders
- Oversee the quality maintenance of TMF documentation
- Provide updates and support to internal project teams

Requirements:

- Bachelor’s degree in Life Sciences or related area
- At least 8 years in clinical research setting
- Proven site activation and management experience
- Knowledge of ICH-GCP guidelines essential
- Excellent organizational and bilingual communication skills

Use your expertise to contribute significantly to AbCellera's mission in advancing breakthrough therapeutics.

📌 Experienced Clinical Start-Up Manager Role (Montreal)
🏢 AbCellera
📍 Montreal