University degree in Law and ideally an LLM. Admission to the Swiss bar or in a European country is preferred. Significant legal experience at a pharmaceutical, biotechnology, medical device or other life sciences company, or experience within a law firm advising such organizations. Experience drafting and negotiating Clinical Trial Agreements with industry sponsors, government agencies, universities and large healthcare companies, as well as agreements such as informed consent forms, confidentiality, regulatory, consulting, supply, and other related clinical trial agreements. Experience in advising on legal and regulatory provisions, especially in dynamic cross functional roles. Experience drafting, reviewing and negotiating a variety of commercial contracts, including but not limited to: vendor agreements, licensing agreements, confidentiality agreements, master service agreements, clinical trial/supply agreements, safety data exchange agreements, laboratory services agreements, consulting agreements, R&D agreements, manufacturing agreements, indemnity agreements, and managed care contracts. Fluency in English needed; German ais a must; any other languages are a plus.