Join GSK as a Regulatory Affairs Manager specializing in Oncology or CMC in Canada. Focus on optimizing approval pathways and enhancing healthcare outcomes through strategic submissions. This hybrid role requires a seasoned regulatory skilled overseeing key oncology or CMC submissions and compliance.
Your leadership will be vital in achieving aggressive approval timelines and competitive labeling, fostering collaboration across global functions. This position is perfect for those ready to innovate in regulatory affairs and impact patient care positively. Key Responsibilities:
Create regulatory strategies for oncology or CMC products
File regulatory submissions meeting ambitious timelines
Ensure adherence to Health Canada and GSK regulatory standards
Build relationships with regulatory agencies to enhance efficiency
Guide and mentor junior team members in regulatory processes Requirements:
B.Sc. in life science or related field
Proven regulatory affairs experience in oncology or CMC
Robust knowledge of Canadian drug regulations
Excellent influencing and leadership skills
Solid commitment to quality and compliance standards Channel your regulatory expertise to elevate GSK's mission to improve patient health in Canada.