Med-in.at is seeking an Associate Director of Regulatory Affairs in Clinical Oncology to lead and supervise oncology projects, ensuring regulatory compliance and effective team collaboration. The ideal candidate will possess extensive experience in regulatory affairs, particularly in oncology, along with strong communication and leadership skills
Job Summary
The Associate Director is responsible for leading regulatory projects within the oncology portfolio and serving as the primary contact for Health Canada.
This role requires a minimum of 10 years of experience in clinical regulatory affairs with specific expertise in oncology product registrations.
The position involves fostering a collaborative global environment while ensuring strict compliance with Canadian laws and company ethics.
Matching Summary
Match Score: 85
Med-in.at is seeking an Associate Director of Regulatory Affairs in Clinical Oncology to lead and supervise oncology projects, ensuring regulatory compliance and effective team collaboration. The ideal candidate will possess extensive experience in regulatory affairs, particularly in oncology, along with strong communication and leadership skills.
Skills & Requirements
Must-have
Health Canada regulatory submissions
Oncology portfolio management
French language proficiency required
Food and Drug Act knowledge
Priority review submission experience
Nice-to-have
Virtual team environment leadership
Cross-cultural collaboration skills
Continuous process improvement mindset
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 Submission filings to Health Canada
Advanced French language skills (written and oral)