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Director, Sr. Corporate Counsel
Refer job# EQAC169130
Director, Senior Corporate Counsel Duties: Serve as lead attorney and strategic advisor on contracts, day-to-day operations and business strategy for the Therapeutics team (ranging from early stage research to clinical phase) and Research team. Draft, structure, and negotiate a variety of commercial agreements, including licenses, supply agreements, manufacturing agreements, service agreements, collaboration agreements, data transfer agreements, development agreements, material transfer agreements, nondisclosure agreements, clinical trial agreements, CRO and other vendor agreements. Advise the Therapeutics and Research teams on legal, regulatory compliance and contractual matters related to drug discovery and development and keep business partners apprised of relevant legal developments and identify training needs and develop and conduct training. Collaborate with key stakeholders, including colleagues in Engineering, Product, Security, Research Ethics, and Regulatory Affairs as well as colleagues across the Legal function, including IP and Privacy to identify and communicate risks. Contribute to legal due diligence procedures and SEC reporting compliance. Manage contracts personnel and contracts function for business, including team members supporting consumer/patient services and research teams; develop and maintain contract templates. Work effectively with external counsel, wherever appropriate, and supervise their work.

Qualifications: JD from an accredited law school in the US and active member of at least one State Bar. Strong scientific background, including an undergraduate degree, in biochemistry, molecular biology, or related science and substantial transactional experience drafting agreements involving biotechnology, biopharmaceutical, or related subject matter. Should have 10 years of in-house corporate legal and/or law firm experience that includes, 5+ years of in-house biotech/biopharma experience; and 3+ years of R&D support relating to a biotech/biopharma drug discovery and development. Technical legal expertise in supply, CRO, pharma/biotech research and development activities, clinical trial agreements, data transfer agreements and complex collaboration and licensing transactions. Experience in daily counseling of research and drug development teams. Excellent verbal and written communicator; delivers concise and clear advice that exhibits strong business judgment and ability to influence others. Excellent organizational and time management skills, able to and thrives handling multiple projects simultaneously. Proven ability to network and build strong working relationships to encourage the routine engagement of counsel. Demonstrated analytical skills as well as the ability to take disparate information and make strategic recommendations quickly.
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