Job Details

Corporate Counsel

Company name

Organization Type


Job Type


Years of Experience

Min 5 yrs required


Foster City, CA

Date Last Verified

Oct 15,2017

Posted on

Aug 10,2017
Practice Area
Corporate >> Corporate - General
Contract Law >> Contract Law
  Employer Sponsored Job (Free to apply to)
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Corporate Counsel Responsibilities: Draft and negotiate a wide range of legal documents typical of a biotech or pharmaceutical research organization including MTAs and research collaborations with academic institutions, agreements with NIH and other governmental entities such as CRADAs, supply agreements, funded research agreements, grant agreements, and various vendor services agreements. Draft and negotiate R&D licensing, development, and collaboration agreements as needed. Advise internal clients on contract interpretation, dispute resolution, IP ownership and other legal risks. Assist with the development of policies and procedures, and standard template language to be used in contracts. Mentor, train and advise contract specialists in the Corporate Legal department on the preparation, negotiation and execution of form-based documents. Work with Corporate Development team and other departments within the company to conduct and coordinate due diligence efforts in strategic transactions as needed. Support other attorneys in the Corporate Legal Group on company transactions and management of existing alliances and partnerships as needed. Work with attorneys in the IP Group in a corporate litigation support function as needed.

Qualification and Experience

Qualifications: JD Degree from a nationally recognized law school. Admitted to practice (preferably in California). BS in life sciences or related field preferred. 5+ years in a law firm and/or in-house advising on, drafting and negotiating agreements, including significant experience with transactions in the biotechnology or pharmaceutical industry. Prior experience with or exposure to agreements with academic institutions and/or the NIH and other governmental entities preferred. Prior experience with or exposure to international regulatory processes for pharmaceutical products and laws and regulations governing clinical trials preferred. Ability to manage and serve a wide range of clients within the company by recognizing and responding quickly and pragmatically to urgent situations and demanding clients. Exceptional and demonstrated written and verbal communication skills. ability to work with and coordinate activities across a large number of individuals across various departments, not only within the company’s headquarters in Foster City, but also throughout the company’s domestic and international subsidiaries in Europe, Latin America and Asia. Appropriately triage a heavy workflow, setting appropriate priorities with clients and delivering results efficiently. Ability to think creatively, devise solutions to challenging problems and effectively drive issues to closure. Exercise mature and reliable judgment while enjoying the company’s enthusiastic, informal and fast-paced environment. Ability to work independently and as a team.

Additional info

Ref. R0000965

Company info

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