Global Regulatory Strategy Director

Daiichi Sankyo US; Basking Ridge (NJ); On-site; USD 193,000 - 290,000; Full time

Job summary

Daiichi Sankyo US in New Jersey seeks a Global Regulatory Lead to shape regulatory strategy for development programs and represent regulatory in GPT meetings. You will guide submissions, align regional plans, and ensure Health Authority alignment across global programs.

Required: 7+ years in regulatory affairs with NDA/BLA experience including the US, and strong cross‑functional leadership in oncology-focused development. Travel up to 20%.

Qualifications

• Bachelor's Degree preferably in a scientific discipline required.
• Advanced degree (e.g., Masters, Pharm.D., Ph.D., MD, JD) preferred.
• Broad and deep scientific and regulatory expertise in early- and late-stage development across modalities and therapeutic areas with focus on oncology.
• Drug Discovery and Development knowledge across the R&D continuum.
• 7+ years of relevant pharmaceutical experience including 5 years of experience in a Strategy role within Regulatory Affairs.
• Hands on NDA/BLA submission experience in a major geographical region, including the US.
• Demonstrated experience in global Health Authority negotiations.
• Manages complexity of regulatory strategy across regions and has the knowledge to provide regulatory guidance based on understanding of global regulations.
• Communicates and collaborates effectively and deals well with ambiguity.
• Working knowledge of CMC and Companion Diagnostics.

Responsibilities

• Manages, directs, and drives the strategy for all regulatory activities associated with the registration and support of new and approved drug products.
• Responsible for ensuring aligned global regulatory strategy is endorsed by the Global Project Team and governance bodies.
• Serves as a leader of the Global Regulatory Team (GRT) and is responsible for strategic integration of regional strategies, including an understanding of CMC, supply chain and commercialization aspects to support Health Authority requirements.
• Serves as the primary point of contact with Alliance Partners Joint-regulatory teams and Joint-GPT.
• Keeps current with latest Health Authority guidelines and provides regulatory advice to members within Regulatory, and other departments within the Company.
• Communicates with outside consultants (i.e. CROs, external partners) as needed.

Education

Bachelor's Degree preferably in a scientific discipline

Advanced degree (e.g., Masters, Pharm.D., Ph.D., MD, JD) preferred

Job description

Daiichi Sankyo US in New Jersey seeks a Global Regulatory Lead to shape regulatory strategy for development programs and represent regulatory in GPT meetings. You will guide submissions, align regional plans, and ensure Health Authority alignment across global programs.

Required: 7+ years in regulatory affairs with NDA/BLA experience including the US, and strong cross‑functional leadership in oncology-focused development. Travel up to 20%.