Key Accountabilities/Responsibilities:Develops regulatory strategies for rapid approvals with optimal labelling for products within therapy or for submissions within specialization areaAccountable for a portfolio of products, specific in the Oncology therapy area, including the preparation, filing and approval of regulatory submissions NDSs, SNDSs, CTAs, NCs, etc to aggressive targetsEnsures compliance with applicable Health Canada, industry, and GSK codes and guidelines in alignment with business needsBuilds trust with Health Canada contacts to improve GSK submission approval times, achieve c...
