Global Clinical Study Manager

Each of us cares about someone who will need medicines. That’s why our vision is to repeatedly beat the odds to deliver breakthrough medicines to patients that need them. We pursue truth and scientific rigour and have the courage to work at the edge of the unknown.

We are seeking a highly motivated and experienced Clinical Study Manager (CSM) to lead and manage clinical trials from start-up through to completion.

Requirements

, protocols, and standard operating procedures (SOPs). In this role, you will collaborate with cross-functional teams, including clinical research associates (CRAs), data managers, and regulatory personnel, to deliver high-quality clinical data while maintaining adherence to the budget and timelines.

and ethical standards, handling regulatory inspections and audits, and implementing corrective actions when necessary Developing and managing project timelines, milestones, and budgets, ensuring all deliverables are met within the agreed-upon timeframe and budget Identifying potential risks to the study, developing mitigation strategies, and taking appropriate action to resolve issues as they arise during the course of the study Overseeing the collection, analysis, and reporting of clinical trial data, ensuring data integrity and quality, accurate data handling, and compliance with data protection regulations Monitoring and ensuring the safety and welfare of study participants by adhering to safety reporting guidelines and promptly addressing any safety concerns We'd love to hear from you if: You have a Master’s degree in a relevant field, and 6+ years of demonstrated work experience as a Regional Clinical Project Manager or Clinical Study Manager; candidates with a Bachelor’s degree and 8+ years of related experience will also be considered You have strong working knowledge of Good Clinical Practice (GCP), regulatory

, and clinical trial management You have previous experience as a CRA, or experience working at clinical sites You have strong organizational and project management skills, with the ability to prioritize and manage competing deadlines You are bilingual with excellent communication skills, both written and verbal, and have the ability to collaborate effectively with internal teams, external vendors, and clinical investigators You are proficient in clinical trial management systems (CTMS), electronic data capture (EDC) systems, and other relevant software You are certified in Clinical Research, such as ACRP, SOCRA (desirable)

What We Offer

: In addition to base salary, we offer equity, annual bonus dependent on team and company performance, and a 6% (non-match) RRSP contribution.

Benefits

Scientific and technical mentorship is a priority. And you’ll find a strong sense of community and connections across AbCellera through our work, clubs, and socials. About AbCellera Creating medicines is the most important work we can do.