Global Regulatory Affairs Manager (Cardio-Metabolic)

Novartis; Greater London; Hybrid; GBP 60,000 - 80,000; Full time

Job summary

A leading pharmaceutical company in London is seeking an experienced Global Program Regulatory Manager to join their team. This critical role involves driving regulatory strategy, managing submissions, and ensuring compliance with global requirements. The ideal candidate will have a Bachelor's or Master's degree in a related field, experience in regulatory affairs, and a strong understanding of drug development processes. Join a collaborative team making impactful contributions to pharmaceutical product commercialization.

Qualifications

• Proven experience in regulatory affairs within the pharmaceutical industry.
• Strong understanding of drug development and clinical trial processes.
• Experience in managing regulatory submissions and Health Authority interactions.

Responsibilities

• Implement regional regulatory strategies in alignment with global objectives.
• Lead interactions with Health Authorities including briefing material preparation.
• Coordinate timely and compliant regulatory submissions across assigned regions.

Skills

Detail-Oriented

Negotiation Skills

Regulatory Compliance

Clinical Trials

Education

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

Tools

Adobe Acrobat

FDA Regulations

Biotechnology

Job description

Job Description Summary

#LI-Hybrid (12 days per month on-site)

Location : London (The Westworks) United Kingdom

Internal Job Title : Global Program Regulatory Manager

We are looking for an experienced and proactive Regulatory Affairs Manager to join our Global Regulatory Affairs team. This role is critical in driving regulatory strategy and managing operational activities across key regions. You will collaborate with cross-functional teams to ensure timely submissions approvals and compliance with global regulatory requirements supporting the successful development and commercialization of pharmaceutical products.

Job Description

Major Responsibilities

• Implement regional regulatory strategies in alignment with global objectives.
• Contribute to global regulatory planning and identify strategic gaps or risks.
• Lead or support Health Authority (HA) interactions including briefing material preparation.
• Coordinate timely and compliant regulatory submissions across assigned regions.
• Review and approve Clinical Trial Applications (CTAs) Investigational New Drugs (INDs) and Risk Management Plans.
• Act as a liaison with local HAs (e.g., FDA EMA) as required.
• Ensure timely and effective responses to HA queries and requests.
• Collaborate cross-functionally to align regulatory plans with business goals.
• Monitor and ensure compliance with internal policies and external regulations.
• Support or lead negotiations for regional approvals to meet project timelines.

Essential Requirements

• Bachelors or Masters degree in Life Sciences Pharmacy or a related field.
• Proven experience in regulatory affairs within the pharmaceutical industry.
• Strong understanding of drug development and clinical trial processes.
• Experience in managing regulatory submissions and HA interactions.

Commitment to Diversity and Inclusion / EEO

Novartis is committed to building an outstanding inclusive work environment and diverse teams representative of the patients and communities we serve.

Skills Desired

Clinical Trials Detail-Oriented Drug Development Lifesciences Negotiation Skills Regulatory Compliance

Required Experience : Manager

Key Skills

• Proofreading,Adobe Acrobat,FDA Regulations,Manufacturing & Controls,Biotechnology,Clinical Trials,Research & Development,GLP,cGMP,Product Development,Chemistry,Writing Skills

Employment Type : Full-Time

Experience : years

Vacancy : 1