Job Number:
HC-03623
Date Posted:
March 8, 2026
Position Title:
Associate Director, Global Regulatory Project Management and Strategic Planning
Party:
N/A
Office Code:
Office/Company:
Takeda Pharmaceuticals
Reports To:
Location:
Remote
Contact:
Salary:
Primary Role
Secondary Role:
Job Type:
Full Time
Description:
At Takeda, we are a forward-looking, world-class R&D organization that unlocks innovation and delivers transformative therapies to patients.Partnership: Partners with the Global Regulatory Lead (GRL) on Global Regulatory Teams (GRTs) to ensure global regulatory project plans for programs / products are established and maintained, and plans & directs the seamless execution of the GRT goals.Bachelor’s degree required (Science emphasis preferred). Advanced degree preferred.
Responsibilities:
• Partners with the Global Regulatory Lead (GRL) on Global Regulatory Teams (GRTs) to ensure global regulatory project plans for programs / products are established and maintained, and plans & directs the seamless execution of the GRT goals.
• Leads cross-functional project submission working groups (SWG) to deliver successful submissions/filings and outcomes with Health Authorities (HA) for early to late phase programs by providing effective Project Management leadership, oversight, direction and planning.
• Directly supports program GRL by ensuring project management and regulatory operational support for the asset is effective, seamless and delivering to expectations.
Qualifications:
• Bachelor’s degree required (Science emphasis preferred). Advanced degree preferred.
• Ideal candidate has a minimum of 8 years related experience (e.g., Regulatory Project Management), preferably with 4 years in Global Regulatory Affairs.
• Experience working on late-stage filings is highly preferred.
Instructions:
Email to apply
Other:
Takeda is a patient-focused company that will inspire and empower you to grow through life-changing work.
