Merck Sharp & Dohme Corp is seeking an Associate Director for Regulatory Affairs in Clinical Oncology, responsible for overseeing oncology projects and submissions to Health Canada. The ideal candidate should have a minimum of 10 years of experience in regulatory affairs, particularly in oncology, and possess strong communication and collaboration skills
Job Summary
The Associate Director will lead regulatory projects within the oncology portfolio.
This role involves significant interaction with Health Canada and global regulatory affairs.
The company values diversity and encourages a collaborative work environment.
Matching Summary
Match Score: 85
Merck Sharp & Dohme Corp is seeking an Associate Director for Regulatory Affairs in Clinical Oncology, responsible for overseeing oncology projects and submissions to Health Canada. The ideal candidate should have a minimum of 10 years of experience in regulatory affairs, particularly in oncology, and possess strong communication and collaboration skills.