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Legal Counsel, Clinical Legal

Job in Jersey City, Hudson County, New Jersey, 07390, USA
Listing for: Gilead Sciences, Inc.
Full Time position
Listed on 2026-02-06
Job specializations:
  • Law/Legal
    Emergency Crisis Mgmt/ Disaster Relief, Regulatory Compliance Specialist
Job Description & How to Apply Below

Overview

Gilead’s Corporate Legal Group is seeking an attorney who thrives in a high-volume, fast-paced, high-performing and collaborative corporate environment. This individual will work within Gilead’s Clinical Legal team, which is responsible for the review, negotiation and management of a variety of agreements in support of Gilead’s clinical trials. This role is part of a five-person team spread across the U.S. and reports to the Clinical Legal team lead.

This position is based with a preference for on-site work in Foster City (CA) or Parsippany (NJ) with a requirement to come into the office at least three times per week. Remote candidates outside of those areas may be considered.

Specific Responsibilities
  • Review and negotiate day-to-day Company agreements including global clinical trial agreements (CTAs), investigator sponsored research agreements, confidentiality, consulting and miscellaneous vendor agreements for a broad range of clients.
  • Draft, review and negotiate these agreements, handling all routine issues and consulting with attorneys in the group when complex legal questions arise.
  • Advise stakeholders and train internal clients on contract forms and procedures.
  • Provide guidance and support to Contracts Specialists within the group.
  • Create resources to ensure internal compliance with Company processes.
Education & Experience Requirements
  • Bachelor’s degree, Juris Doctorate and hold active bar license in at least one state.
  • Experience should include drafting and negotiating clinical contracts in a bio-pharma company, university or Contract Research Organization.
  • 4+ years experience drafting and negotiating clinical trial agreements in a variety of countries.
  • Experience with or knowledge of Pharma contract issues that overlap with FDA regulations.
  • Experience collaborating with government agencies and non-profits.
  • Experience with or knowledge of data privacy laws foreign (e.g. GDPR) and domestic.
  • Experience with or knowledge of intellectual property contract issues.
  • The ideal candidate will be flexible and willing to learn new procedures and skill sets.
  • Must have excellent organizational skills, attention to detail and the ability to perform in a fast-paced, deadline-driven environment.
  • Creative and solution-driven mindset.
  • Ability to multi-task and handle multiple contract negotiations simultaneously.
  • Must be able to set and appropriately modify priorities with internal clients on an ongoing basis and manage client and third party expectations.
  • Must be capable of analyzing legal issues and have comfort in advising client groups on various legal issues related to contracting.
  • Ability to work independently and as part of a team.
  • Must be able to collaborate and work with other departments such as Clinical Operations, Clinical Development, Risk Management, Regulatory, and Compliance.
  • Strong oral and written communication skills.
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