Associate Director Transactional Law

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Associate Director Transactional Law
The candidate negotiates and drafts contracts related to clinical trials, including Company-sponsored clinical trial agreements, CRO agreements, IST agreements, and vendor agreements. Negotiates and drafts HCP agreements. Reviews and advices on informed consent forms and authorizations. Provides legal interpretation on clinical agreements, vendor agreements informed consents and authorizations and other related business matters. Provides supervision and management of members of the Transactional Law Clinical team, including employees and contractors. Advises on matters that relate to compliance with international regulations and standards pertaining to clinical development and data privacy. Interfaces with external legal resources, as needed. Other responsibilities as assigned. Should have a law degree and 7 years of relevant legal experience, including experience as in-house counsel. Experience in a fast-paced, entrepreneurial environment is critical, as is the ability to “roll up sleeves” and work in a hands-on manner. Experience in the pharmaceutical/biotechnology industry is required. Experience developing processes and standards to ensure contract management efficiency. Extensive experience working with clinical development, in North America (mandatory), Asia-Pacific (mandatory), and the rest of the world (preferred) regions. Computer proficiency including Microsoft Word, Excel, and PowerPoint. High command of English is mandatory, and a second language is preferred.

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