Description

You will draft, review, and negotiate various commercial contracts for pharmaceutical and life science clients, and advise directly on regulatory matters such as MHRA/EMA marketing. This role offers flexibility to work remotely, onsite, or hybrid based on client needs.

Requirements

• 2 to 15 years post-qualification experience at a pharmaceutical, biotech, medical device or life sciences company or law firm advising pharma clients
• Experience in regulatory matters including MHRA/EMA marketing
• Good academic credentials and UK legal qualification
• Strong commercial understanding and excellent interpersonal skills
• Right to work and eligible to practice as a lawyer in the UK

Responsibilities

• Draft, review and negotiate commercial contracts including vendor, licensing, confidentiality, clinical trial, supply, and service agreements
• Advise corporate clients on regulatory matters including MHRA/EMA marketing (advertising, promotion, labelling)
• Provide entrepreneurial, pragmatic, business-oriented legal advice
• Work in a fast-paced environment with professionalism and business judgment