Global Regulatory Lead (Cardio‑Metabolic) – Hybrid

Novartis; Greater London; Hybrid; GBP 70,000 - 90,000; Full time

Job summary

A leading pharmaceutical company is seeking a Senior Global Program Regulatory Manager to lead regulatory strategies and operational activities. The ideal candidate will have extensive experience in regulatory affairs, a strong background in project management, and excellent problem-solving skills. Fluency in English is essential. This role is based in London with a hybrid working model. Responsibilities include managing submissions, ensuring compliance, and overseeing Health Authority interactions to expedite regulatory approvals.

Qualifications

• Significant experience in regulatory affairs within the pharmaceutical industry.
• Proven track record in project management and regulatory operations.
• Fluency in English (written and spoken) is essential.

Responsibilities

• Lead the implementation of regulatory strategies and operational activities across major global regions.
• Align regional regulatory approaches with global objectives through collaboration.
• Develop and implement strategies to minimize review delays and regulatory clock stops.

Skills

Clinical Trials

Cross-Functional Teams

Detail-Oriented

Drug Development

Lifesciences

Negotiation Skills

Problem Solving Skills

Regulatory Compliance

Risk Management

Education

Bachelors or Masters degree in Life Sciences, Pharmacy, or a related field

Tools

Adobe Acrobat

Job description

A leading pharmaceutical company is seeking a Senior Global Program Regulatory Manager to lead regulatory strategies and operational activities. The ideal candidate will have extensive experience in regulatory affairs, a strong background in project management, and excellent problem-solving skills. Fluency in English is essential. This role is based in London with a hybrid working model. Responsibilities include managing submissions, ensuring compliance, and overseeing Health Authority interactions to expedite regulatory approvals.