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 professional 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
- Strong 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.