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Oncology Regulatory Affairs Director
vor 2 Monaten
Company Overview:
Daiichi Sankyo is a global leader in the pharmaceutical industry with over 120 years of expertise and a workforce exceeding 17,000 across more than 20 nations. Our commitment lies in the discovery, development, and delivery of innovative healthcare solutions that enhance the quality of life worldwide.
Focus Areas:
In Europe, our Specialty Business is dedicated to combating cardiovascular diseases, which are the primary cause of mortality in the region. Concurrently, our Oncology division aims to position itself as a frontrunner in pharmaceutical innovation, focusing on the creation of groundbreaking therapies for cancer patients.
Position Overview:
We are currently seeking a highly skilled professional for the role of Director Regulatory Affairs Oncology. This position will provide strategic regulatory support across Europe for various projects and products, as well as non-project-related activities.
Key Responsibilities:
- Develop and implement European regulatory strategies for assigned oncology projects.
- Serve as a regulatory expert within the oncology domain, collaborating with internal teams across Europe and globally.
- Represent Regulatory Affairs in external engagements, including interactions with regulatory authorities, affiliates, partners, and contract research organizations (CROs).
- Provide regulatory expertise to support regional and global objectives.
This role is pivotal in ensuring that our oncology initiatives align with regulatory requirements while advancing our mission to deliver innovative cancer therapies.