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
• Robust influencing and analytical skills
Leverage your regulatory expertise to enhance AstraZeneca's high-quality deliverables and make a lasting impact.
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