• Developing clinical, technical, and regulatory operational documents for health authorities, as well as internal and external stakeholders.• Interviewing departmental heads/employees and discussing feasibility.• Assisting in constructing and maintaining a document management system for the Quality Assurance department.• Ensuring language is clear and concise, formatting in compliance with QA standards. • Actively participating in an environment that fosters safety, quality and continuous improvement in best practice and quality research.

• Assisting in preparing, submitting and maintaining all clinical trial applications submitted to the local Research Ethics Board (REB).• Working collaboratively with UBC REBs along with various other local, provincial and national regulatory, academic and health bodies. • Assisting in the day-to-day administrative processes related to research ethics. Acting as a liaison between research teams, relevant ethics committees, sponsors and PIs. • Practicing critical and analytical thinking in response to activities involved in clinical research study start-up and maintenance.• Working closely with members of a research team to ensure issues are quickly and appropriately resolved to retain scientific integrity and protect patient safety.