Global Regulatory Submissions PM Leader

Ipsen Group; Greater London; On-site; GBP 80,000 - GBP 120,000; Full time

Job summary

A leading biopharmaceutical company is seeking a Head of Regulatory Submission Project Management to oversee global submissions, ensure high-quality delivery, and lead a dedicated team. The ideal candidate will have 10-15 years of experience in regulatory affairs, demonstrating strong leadership, strategic thinking, and the ability to manage complex projects. This position offers an opportunity to make a significant impact on the company's success and the lives of patients needing innovative therapies.

Qualifications

• Significant experience in the pharmaceutical or biotechnology industry.
• Extensive regulatory submission and project management experience.
• Strong ability in portfolio/program management and risk-based decision support.

Responsibilities

• Lead a unified Regulatory Project Management organization for submissions.
• Define and implement submission strategies aligned with business objectives.
• Provide oversight for high-priority and complex submissions.

Skills

Strategic leadership

Regulatory project management

Risk management

Communication

Cross-functional collaboration

Education

Minimum 10-15 years in Regulatory Affairs/Pharmaceutical Project Management

Job description

A leading biopharmaceutical company is seeking a Head of Regulatory Submission Project Management to oversee global submissions, ensure high-quality delivery, and lead a dedicated team. The ideal candidate will have 10-15 years of experience in regulatory affairs, demonstrating strong leadership, strategic thinking, and the ability to manage complex projects. This position offers an opportunity to make a significant impact on the company's success and the lives of patients needing innovative therapies.