The Associate Director of Regulatory Affairs for Clinical Oncology at leHACK is responsible for overseeing regulatory projects and submissions related to oncology products. The ideal candidate should have over 10 years of experience in regulatory affairs, particularly within oncology, and must possess strong communication and collaboration skills
Job Summary
The Associate Director leads regulatory projects within the oncology portfolio, including planning and assigning key tasks to specialists.
This role serves as the primary contact for Health Canada regarding the oncology portfolio and represents the company in global regulatory meetings.
The position requires a candidate with at least 10 years of experience in clinical regulatory affairs and a demonstrated ability to work independently with minimal supervision.
Matching Summary
Match Score: 85
The Associate Director of Regulatory Affairs for Clinical Oncology at leHACK is responsible for overseeing regulatory projects and submissions related to oncology products. The ideal candidate should have over 10 years of experience in regulatory affairs, particularly within oncology, and must possess strong communication and collaboration skills.
Salary
Not specified; Not specified; Not specified
Skills & Requirements
Must-have
Health Canada regulatory submissions
Oncology clinical regulatory expertise
French language proficiency required
New product registration experience
Stakeholder management with Health Canada
Nice-to-have
Virtual team environment leadership
Continuous process improvement focus
Cross-cultural collaboration skills
Strategic thinking in oncology
Change management initiatives
Key Requirements
Minimum 10 years regulatory affairs experience
M.Sc. or higher in Health Sciences
Completed New Drug Submissions to Health Canada
Fluent French (written and oral)
Experience in oncology clinical regulatory affairs