Signatory Lead

Novartis UK; Greater London; Hybrid; GBP 68,000 - 126,000; Full time

Benefits offered by this job

Insurance plans

Retirement plans

Wellbeing resources

Global recognition programs

Flexible and hybrid working options

Minimum 14 weeks paid parental leave

Company vehicle or car allowance

Job summary

Novartis UK is seeking a Signatory Lead to ensure promotional and non-promotional materials comply with the ABPI Code and Novartis policies. You will act as the final medical signatory, guiding code matters and enabling informed risk management across the organisation.

You will partner with Medical, Commercial, ERC and other stakeholders to drive strategy, content review, and lifecycle governance, ensuring scientific robustness and high-quality outputs aligned with business objectives.

Qualifications

• University degree in life sciences, marketing, business, or a related field.
• GMC registered Physician or GPhC registered Pharmacist.
• English language proficiency required. Country language knowledge as applicable.

Responsibilities

• Acts as the final medical signatory for allocated therapy areas, advising on ABPI Code, regulations, and Novartis policies.
• Reviews and certifies promotional and non-promotional materials within approval systems, ensuring accuracy and risk management.
• Provides pragmatic, risk-based advice to support business objectives and maintain governance.

Skills

ABPI knowledge

Medical affairs

Stakeholder management

Regulatory compliance

Education

GMC registered Physician

GPhC registered Pharmacist

Job description

Summary

The Signatory Lead is accountable for ensuring that promotional and non-promotional materials and activities comply with the ABPI Code of Practice, The Signatory Lead is accountable for ensuring that promotional and non-promotional materials and activities comply with the ABPI Code of Practice, applicable regulations, and Novartis policies. Acting as a final medical signatory, they provide expert guidance on code and compliance matters, enabling informed decision-making and effective risk management across the organisation. The Signatory Lead partners closely with Medical, Commercial, ERC and cross-functional stakeholders throughout the lifecycle of projects, contributing to strategy development, content creation, review and approval processes, and governance activities to ensure materials are scientifically robust, high quality, compliant, and aligned with business objectives.

Summary

The Signatory Lead is accountable for ensuring that promotional and non-promotional materials and activities comply with the ABPI Code of Practice, The Signatory Lead is accountable for ensuring that promotional and non-promotional materials and activities comply with the ABPI Code of Practice, applicable regulations, and Novartis policies. Acting as a final medical signatory, they provide expert guidance on code and compliance matters, enabling informed decision-making and effective risk management across the organisation. The Signatory Lead partners closely with Medical, Commercial, ERC and cross-functional stakeholders throughout the lifecycle of projects, contributing to strategy development, content creation, review and approval processes, and governance activities to ensure materials are scientifically robust, high quality, compliant, and aligned with business objectives.

About The Role

Major Accountabilities

• Acts as the final medical signatory for allocated therapy areas, providing expert guidance on the ABPI Code of Practice, relevant regulations, and Novartis policies, and serving as the primary point of contact for code and compliance advice.
• Responsible for the review and certification of promotional and non-promotional materials and activities within Novartis approval systems, ensuring compliance, scientific accuracy, and appropriate risk management.
• Acts as a subject matter expert on the ABPI Code of Practice, industry regulations, and internal governance requirements, providing pragmatic, risk-based advice to support business objectives.
• Partners closely with Medical, Commercial, ERC and cross-functional stakeholders to co-create strategies, projects and tactical plans, embedding compliance considerations from concept through to approval, implementation and lifecycle management.
• Supports the management of PMCPA complaints, audits and inspections, contributing to root cause analysis, corrective actions and continuous improvement initiatives.
• Drives quality and consistency in review and approval activities by sharing best practice, coaching stakeholders, and providing constructive feedback to enhance compliance standards across the organisation.
• Builds and maintains effective relationships with external vendors and service providers, identifying opportunities to optimise processes, quality, efficiency and compliance.
• Collaborates with Signatory and Ethics, Risk & Compliance colleagues to promote consistent, enterprise-wide approaches to governance, decision-making and materials review.
• Identifies and implements process improvement opportunities that enhance operational efficiency, simplify ways of working and improve stakeholder experience while maintaining compliance.
• Effectively prioritises workload and adapts to changing business needs, demonstrating agility and resilience in a dynamic environment.
• Role models Novartis values, culture and behaviours, fostering collaboration, accountability, innovation and a patient-focused mindset.

Key Performance Indicators

• Compliance with ABPI code of Practice / other industry regulationsand Internal Novartis Policies
• Approval of Novartis Materials within timelines specified within Novartis SOPs
• No critical deviations from Novartis policies, processes, SOPs/WPs/FRMs
• Audit & Inspection readinessat all times.
• Compliance with Novartis Information Security
• Training completed and up to date with 98% compliance.

Ideal background

• University degree in life sciences, marketing, business, or a related field.
• GMC registered Physician orGPhCregistered Pharmacist
• English
• Country language required

Relevant Experiences

• Significant experienceinMedicalaffairs in a final signatory role or relevant skills and experience to become a registered signatory in a shorttimeframe.
• Experience in PMCPA code complaints beneficial
• Strongunderstanding of the ABPI codewith a solutions-oriented approach to the grey areas
• Demonstrates a customer-focused mindset.
• Good Enterprise & Strategic mindset with courage to challenge status quo.
• Innovative and creative approach to complex problem solving and confidence to make decisions.
• Hassolutionorientated mindset and can effectivelyidentifyand overcome challenges but remain flexible to evolving needs of business.
• Strong communication, interpersonal and influencing skills
• Good planning andorganisationalskills
• Able to adapt, organize, prioritize, and work effectively and collaboratively in multifunctional team

Benefits & Rewards

At Novartis, we’re committed to reimagining medicine together - and rewarding the people who make it happen.

Expected Annual Base Salary Range for role:

67,900.00 - 97,000.00 - 126,100.00 GBP Annual

The base salary offered is determined based on gender-neutral objectives, such as relevant skills, competencies and experience in accordance with the Novartis pay setting policy and upon joining Novartis will be reviewed periodically.

In addition to your base salary, you may be eligible for a performance-based bonus depending on certain performance parameters.

The rewards of being part of our team go far beyond base pay and incentives. We also offer a variety of competitive benefits in kind to help you thrive personally and professionally, such as insurance plans, retirement plans, wellbeing resources and global recognition programs. In addition, we provide flexible and hybrid working options, where possible, and minimum 14 weeks paid parental leave.

You may be eligible for a company vehicle or a car allowance in accordance with the applicable local Novartis policies and guidelines.

Pay equity is a fundamental principle of our employment policy and reflects our commitment to create a diverse, equitable and inclusive environment that treats all employees with dignity and respect, as outlined in our Code of Ethics.

Read our brochure to learn more about our global total rewards offering:

https://www.novartis.com/sites/novartis_com/files/novartis-life-handbook.pdf

Note: Benefits and compensation may vary by country and are subject to local legal requirements, including provisions of collective bargaining agreements where applicable. A full overview of your compensation package, including any relevant collective bargaining agreement details applicable to your role based on your employment location and Novartis employer entity, will be communicated separately to you during the application process.

Why Novartis:

Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture

Benefits and Rewards:

Learn about all the ways we’ll help you thrive personally and professionally.

Read our handbook (PDF 30 MB)