At CNX Therapeutics, we’re building a growing European pharmaceutical business with a clear ambition: to improve access to medicines that make a meaningful difference to patients’ lives. With a diverse portfolio and an expanding global footprint, we’re continuing to grow through both our existing business and new opportunities.

Our people are central to this journey. We’re a collaborative, entrepreneurial and fast-moving organisation where individuals have the opportunity to take ownership, make an impact and help shape how we grow. Joining CNX means becoming part of an ambitious team at an exciting stage of our development, with the opportunity to contribute to both our business and the patients we ultimately serve.

The Opportunity

Are you a medical compliance leader ready to shape the governance framework of a growing organisation? We're looking for a fractional Head of Medical Compliance, Governance & Diligence to lead oversight of our medical compliance, governance and scientific review activities ensuring the highest standards of regulatory, ethical and industry code compliance across all promotional, scientific and external engagement work.

You'll take ownership of our medical governance framework, including medical compliance procedures, ABPI Code compliance and promotional review processes, shaping how we operate at every level. Beyond governance, you'll play a strategic role in business development, licensing and acquisition activity; providing medical due diligence, therapeutic assessment and product portfolio evaluation to support our growth.

What You’ll Be Doing

• Establish, maintain and continuously improve the Company's Medical Compliance and Governance Framework, including ownership of Medical Compliance SOPs, policies and governance processes, ensuring they remain current, effective and aligned with regulatory and industry expectations.

• Act as the Company's lead medical compliance professional, providing independent medical oversight of promotional, scientific and external engagement activities.

• Lead and oversee compliance with applicable pharmaceutical industry codes of practice, ethical standards and internal medical governance requirements, including the ABPI, EFPIA and relevant local market codes where applicable.

• Act as Medical Signatory and provide medical review and approval of promotional and non-promotional materials, ensuring all communications are scientifically accurate, balanced and compliant.

• Provide medical and scientific leadership to Commercial, Regulatory, Quality and Senior Leadership teams, supporting informed decision-making across the product portfolio.

• Provide medical leadership and oversight for interactions with healthcare professionals, healthcare organisations, key opinion leaders, professional societies, patient organisations and other external stakeholders, ensuring activities are scientifically robust, compliant and supported by appropriate governance processes.

• Provide medical oversight of relevant promotional, scientific and medical activities conducted by distributors, partners and third-party service providers on behalf of the Company.

• Provide medical leadership and expertise to business development, licensing, acquisition, product launch and portfolio optimisation activities through medical due diligence, therapeutic area assessment, portfolio evaluation, independent clinical risk assessment and review of investigator-sponsored research proposals where appropriate.

• Provide medical assessment and guidance relating to significant product quality issues, market actions, shortages, product complaints, product liability matters and other events with potential patient impact.

• Support the management of pharmaceutical industry code complaints, competitor challenges and compliance investigations, providing medical and scientific expertise as required.

• Establish and deliver a Medical Compliance training programme, ensuring employees and third-party partners understand their responsibilities under internal procedures and industry codes.

• Monitor emerging medical, regulatory and industry developments, assessing potential impacts on the Company's products, activities and strategic objectives.

• Establish appropriate medical compliance metrics, monitoring and reporting mechanisms, providing regular updates to Executive Leadership on compliance performance, risks and emerging trends.