2 to 10 years post-qualification experience at a pharmaceutical, biotechnology, medical device or other life sciences company, or experience in a law firm advising pharma / life science clients.
Experience providing legal advice for a wide range of regulatory matters, including MHRA/EMA marketing (advertising, promotion, labelling).
Good academic credentials and post-qualification experience.
Strong commercial understanding, and excellent interpersonal skills.
Responsibilities:
Drafting, reviewing and negotiating a variety of commercial contracts
Working with and advising corporate clients directly, as well as the ability to provide entrepreneurial, pragmatic, business-oriented advice.
Working in a large, fast-paced environment with a high level of professionalism and outstanding business judgment.