Associate Director, Global Regulatory Affairs
Greater Boston
In this opportunity, you would have the chance to work for a world leading, global pharmaceutical company! Located just north of Boston, this company focuses on neurology & immunology, fertility, endocrinology, and oncology.
Job Responsibilities
- Oversee regulatory submissions ensuring timely preparation of all regulatory documentations at different Regulatory milestones
- Develop and provide regulatory strategies for various regulatory projects
- Aid in the development of risk assessment
Qualifications
- Degree in a Life Science field or related discipline
- 8+ years of regulatory affairs experience
- Oncology experience (highly preferred)
- Clinical trial phase of development experience (IND / CTA / eCTD requirements)