Join a growing biopharmaceutical organization advancing therapies for patients with serious and rare diseases. The Legal Department supports global clinical development initiatives in partnership with clinical operations, research teams, and external stakeholders. This role is part of a collaborative, fast-paced clinical contracting team supporting an active global clinical development pipeline. The successful candidate will independently manage complex clinical trial agreements, navigate international contracting requirements, and support high-volume contracting workflows. This is a part-time contract opportunity of approximately 20 hours per week, with a contract duration of approximately seven months. The schedule will initially vary according to contracting demand and requires responsiveness throughout the workweek; a more structured schedule may become possible as the engagement progresses. The position is based in Bridgewater, New Jersey, but onsite, hybrid, or remote arrangements have not been confirmed. Engagement is W2 only, with no C2C or 1099 arrangements. The role involves drafting, reviewing, negotiating, and completing clinical trial agreements and related documentation for US and international studies; coordinating with internal and external stakeholders; managing agreement execution and records; monitoring shared contracting inboxes; and supporting reporting and operational improvements.
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Job Type
Part-time
Career Level
Senior
Education Level
Ph.D. or professional degree