Elevate your regulatory expertise with AstraZeneca as a Regulatory Affairs Manager on a 9-month contract. You will lead regulatory submissions and strategies while collaborating in a energetic environment. As a Regulatory Affairs Manager, you will bring 2-4 years of regulatory experience in the biopharmaceutical sector or health authority.
This role requires strong project management skills and an understanding of drug development processes. You will oversee regulatory submission strategies and contribute significantly to project delivery plans across global and regional frameworks. Key Responsibilities:
- Lead end-to-end planning for regulatory submissions
- Analyze regulatory procedures and special designations
- Review key documents like study protocols and PSRs
- Coordinate status updates while managing project plans
- Identify regulatory risks and propose mitigation strategies Requirements:
- University Degree in Science or related field
- 2-4 years Regulatory Affairs experience
- Strong project management and leadership skills
- Knowledge of drug development and AZ processes
- Cultural awareness and excellent communication skills Bring your regulatory knowledge and project management skills to AstraZeneca and drive impactful solutions in healthcare.