The Ideal Candidate:
- Team Player
- Adaptable
- Detail Oriented
- Problem Solver
What You'll Do:
- Act as a legal advisor to business stakeholders, exercising sound judgement in interpreting and applying relevant laws, regulations, company policies and procedures.
- Assist with the overarching embedding and maximising the use of AI within Legal whilst maintaining compliance.
- Serve as a key partner to the Global Head of Legal, providing insight, recommendations, and legal risk assessments to support strategic business decisions.
- Lead the drafting, negotiation and management of agreements, including but not limited to master services agreements, vendor service agreements, Statement of Work, Letter of intent, clinical trial agreements, customer agreements, and sub-distribution agreements; provide support to the data privacy paralegal with GDPR agreements.
- Influence and guide internal stakeholders, proactively identifying legal issues and advising on risk mitigation approaches across commercial, operational, and regulatory matters.
- Undertake legal support, including legal research and proofreading.
- Provide support and assistance for continuous improvement of legal templates, contract processes, policies and legal operations.
- Act as a trusted escalation point for contract, commercial and operational legal matters, helping to reduce dependency on the Global Head of Legal for routine issues while ensuring timely escalation of material risks.
- Provide practical, business-focused legal advice that enables faster decision-making, supports revenue-generating activity and helps embed a proactive, solutions-orientated legal service across the organisation.
What You'll Need:
- Qualified with demonstrable senior-level experience in commercial and pharmaceutical / life science legal matters.
- Proven ability to lead commercial negotiations and manage high-value contractual relationships across global markets
- 3-5 years of experience in the pharmaceutical/life sciences sector and at least 2 years of commercial experience.
- Strong track record advising senior leadership and influencing cross-functional stakeholders
- Company secretarial experience.
- Awareness of AI and how it can support legal.
- Global awareness of Data Privacy, as well as GDPR experience;
- Experience in drafting and negotiating general commercial agreements as listed above.
- Track record of leading planning processes with excellent organisational and collaboration skills.
- Proven ability to influence, (appropriately) challenge and engage diverse stakeholders.
- Proven legal analytical and drafting skills, with excellent command in both verbal and written English.
Skills Required
- Qualified with demonstrable senior-level experience in commercial and pharmaceutical / life science legal matters
- Proven ability to lead commercial negotiations and manage high-value contractual relationships across global markets
- 3-5 years of experience in the pharmaceutical/life sciences sector and at least 2 years of commercial experience
- Strong track record advising senior leadership and influencing cross-functional stakeholders
- Company secretarial experience
- Awareness of AI and how it can support legal
- Global awareness of Data Privacy, including GDPR experience
- Experience drafting and negotiating general commercial agreements (MSAs, vendor agreements, SOWs, LOIs, clinical trial agreements, customer agreements, sub-distribution agreements)
- Track record of leading planning processes with excellent organisational and collaboration skills
- Proven ability to influence, appropriately challenge and engage diverse stakeholders
- Proven legal analytical and drafting skills, with excellent verbal and written English
What We Do
We are a rapidly growing niche pharmaceutical services company operating in four key sectors:- Managed Access Programs (MAP) Unlicensed Medicines Access Clinical Trial Sourcing Reference Product Supply. Our goal is to provide positive measurable outcomes to patients and sponsors but above all else we want to be known as your “trusted partner” and an extension of your team. •UK headquarters established in London in 2008. •US Headquarters established in Research Triangle Park, North Carolina in 2012. •Our team has many years of pharmaceutical, clinical and regulatory experience gained in companies such as Pfizer, AZ, MSD, GSK, UDG Healthcare, Waymade, Sanofi, Quintiles & Walgreens Boots Alliance. •Our facilities have been inspected & licensed by the MHRA, UK Home Office, FDA and all necessary local approval bodies. •We are also approved to handle and distribute controlled substances. •We are compliant with all relevant GMDP regulations and operate to a high standard of medicines supply. •We operate under a comprehensive Quality Management System with robust and compliant standard operating procedures (SOPs) and policies. •Our customers and partners include Pharma, Biotechs, Generic and Biosimilar Developers, CROs and Healthcare and Hospital authorities. •We are fully committed to a culture of continual development and strive to service our partners needs beyond their expectations We would be happy to answer any questions that you may have regarding WEP Clinical and our products and services.

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