Join AstraZeneca as a Regulatory Affairs Manager, specializing in project management within regulatory affairs on a 9-month contract. Contribute to impactful regulatory submissions in a collaborative setting.
This position requires a relevant science degree and 2-4 years of regulatory experience, offering a chance to guide submission strategies and improve processes. You will work closely with cross-functional teams and engage with health authorities while managing procedures for various applications. Your analytical skills will be essential in identifying risks and enhancing documentation practices.
Key Responsibilities:
• Manage regulatory submission processes from strategy to delivery • Liaise with health authorities and document key requirements • Prepare and review documents for regulatory compliance • Develop and maintain submission delivery plans • Provide mentoring and support within team initiatives
Requirements: • Relevant University Degree in Science • 2-4 years of industry regulatory experience • Sound knowledge of drug development • Proven project management capabilities • Solid influencing and analytical skills
Leverage your regulatory expertise to enhance AstraZeneca's high-quality deliverables and make a lasting impact. #J-18808-Ljbffr