• Processed, evaluated and submitted reportable adverse events according to Health Canada regulations: narrative writing, severity grading and causality assessment• Prepared and approved annual summary reports• Provided technical medical expertise and drug information in response to enquiriesfrom patients, healthcare professionals and sales representatives•Prepared and filed submissions in compliance with Health Canada requirements using eCTD format• Prepared and reviewed product monographs and labeling materials

• Managed data collection, ensuring accuracy and consistency of clinical data• Handled and processed biospecimens and organized sample repositories• Planned, modified and executed research techniques and tests such as flow cytometry, cell culture and ELISA• Prepared and presented research data at scientific meetings• Assisted in writing and revising manuscripts

• Educated patients on possible drug interactions, potential side effects and optimal methods of administration• Collaborated with store manager to maintain daily operations• Implemented new procedures to follow up on patient compliance with treatment (pillpack, patient-tailored monthly phone calls etc.)• Maintained pharmaceutical stock, created inventories and ordered all pharmacy supplies• Applied policies and procedures for effective pharmacy management such as daily and monthly reports