Advance your career as a Regulatory Affairs Manager at AstraZeneca, where you’ll oversee regulatory projects on a challenging 9-month contract. Drive excellence in regulatory submissions while working collaboratively.

In this role, you will need a background in science and 2-4 years of regulatory experience in the biopharmaceutical industry. Your responsibilities include developing strategic submission plans and ensuring compliance with health authority requirements. As a project manager, you will lead cross-functional teams, analyze regulatory risks, and mentor fellow professionals.

Key Responsibilities:
• Lead planning and execution of regulatory submissions
• Review and refine documents for submission accuracy
• Analyze and recommend strategies for health authority interactions




• Update and maintain project plans effectively
• Coach and support team members in regulatory processes

Requirements:
• Relevant University Degree in a scientific discipline
• 2-4 years of Regulatory Affairs experience
• Robust leadership and project management skills
• Knowledge of AZ processes and drug development
• Excellent communication and analytical abilities

Utilize your regulatory insights and project management acumen at AstraZeneca to foster innovation and collaboration in healthcare solutions.
#J-18808-Ljbffr

📌 Regulatory Affairs Manager Contract at AstraZeneca (Ontario)
🏢 AstraZeneca
📍 Ontario