Senior Legal Counsel
Job Description
Senior Legal Counsel (Associate Director) – Pharmaceuticals
\n📍 Reading (Hybrid, 3 days onsite)
\nAbout the Business
\nBritannia Pharmaceuticals is a UK-based specialty pharmaceutical company that develops and markets medicines for chronic neurological disorders, with a primary global focus on Parkinson's disease. They also offer specialized nursing and support services for patients and their caregivers
\nKey Purpose
\nTo provide commercially focused, pragmatic legal support, acting as a trusted advisor to senior stakeholders while managing legal risk in a highly regulated pharmaceutical environment.
\nThe role will support day-to-day legal needs across commercial contracting, regulatory advisory, and governance, while building capability within a small, high-impact legal team.
\nMain Responsibilities
\n- \n
- Provide legal support across a broad range of commercial and operational matters \n
- Draft, review and negotiate a variety of commercial agreements, including: Supply, procurement and services contracts, HCP and consultancy agreements, pharmacovigilance (PV) agreements, and strategic partnerships and collaborations \n
- Support business stakeholders on regulatory and compliance matters, including: Pharmaceutical regulation, ABPI Code of Practice / PMCPA requirements, and GxP frameworks (GMP, GMDP, PV) \n
- Provide oversight and input on data protection and governance, including GDPR compliance and risk management \n
- Assist with risk identification, issue-spotting and escalation of material legal issues \n
- Act as a business partner to commercial and medical teams, enabling effective and compliant decision-making \n
- Coordinate with global legal teams to ensure consistency of approach across jurisdictions \n
- Manage relationships with external counsel where required \n
- Contribute to process improvements, including contract templates, training, and legal operations \n
Scope and Complexity
\n- \n
- Operates within a lean legal team, requiring a high level of autonomy and ownership \n
- Broad remit spanning commercial, regulatory, and governance matters \n
- Exposure to multi-entity UK operations and international legal interactions \n
- Hands-on role covering the full lifecycle from NDAs through to complex negotiations \n
- Opportunity to develop expertise in pharmaceutical regulatory frameworks and stakeholder partnership within a global organisation \n
Competencies
\n- \n
- Strong commercial contracting and drafting skills \n
- Practical, solutions-focused approach with sound risk judgement \n
- Ability to operate effectively in a fast-paced, regulated environment \n
- Strong stakeholder management and communication skills \n
- Ability to balance business objectives with legal and compliance requirements \n
- Comfortable working autonomously within a small team \n
Qualifications / Experience
\n- \n
- Qualified solicitor (England & Wales or equivalent) \n
- Minimum 5 years PQE required \n
- Proven experience within pharmaceutical or life sciences sector (essential) \n
- Strong knowledge of: ABPI / PMCPA frameworks, pharmaceutical regulation, and commercial contract law \n
- Experience working within matrixed or international organisations desirable \n
You’ll play a key role in supporting a growing UK platform within a global pharma group, with direct exposure to senior stakeholders and international legal teams.
\nIf you’re a pharma-focused lawyer looking for a broad, impactful in-house role, please get in touch for a confidential discussion.
