
501 - 1000 employees
🏥 Healthcare
💼 Consulting
🏭 Manufacturing
Healthcare • Consulting • Manufacturing
ImmunityBio, Inc. is a biotechnology company focused on developing innovative immunotherapies to enhance the immune system's ability to fight cancer and infectious diseases. By harnessing the power of the body’s immune response, ImmunityBio aims to provide breakthrough treatments that can improve patient outcomes and longevity in challenging diseases.
🕒 July 2
🇺🇸 United States – Remote
💵 $77 - $97 / hour
⏰ Full Time
🟡 Mid-level
🟠 Senior
⚖️ Legal Counsel / General Counsel
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501 - 1000 employees
🏥 Healthcare
💼 Consulting
🏭 Manufacturing
Healthcare • Consulting • Manufacturing
ImmunityBio, Inc. is a biotechnology company focused on developing innovative immunotherapies to enhance the immune system's ability to fight cancer and infectious diseases. By harnessing the power of the body’s immune response, ImmunityBio aims to provide breakthrough treatments that can improve patient outcomes and longevity in challenging diseases.
• Draft, review, and negotiate complex CTAs, master service agreements (MSAs), confidentiality agreements, material transfer agreements, and vendor service agreements. • Ensure all clinical trial contracts and processes comply with applicable laws and regulations. • Collaborate with internal stakeholders to develop, update, and maintain standard agreement templates. • Identify potential legal risks within contractual agreements and offer mitigation strategies. • Stay current with changes in legislation and regulatory environments affecting clinical research.
• Juris Doctor degree from an accredited law school is required. • Active member of a State Bar Association (preferably California) required. • 5+ years of experience at a large law firm and/or the legal department of a Life Sciences or Pharmaceutical company required. • Understanding of statutes, regulations, and industry standards governing GxP, clinical research, trial transparency, and product commercialization. • Demonstrated expertise in drafting and negotiating clinical trial-related agreements and a strong understanding of the clinical development process. • Proven ability to handle a wide range of general corporate and commercial contracts beyond the clinical context. • In-depth knowledge of federal, state, and, preferably, international laws and regulations governing clinical research (e.g., FDA, GCP, ICH guidelines, data privacy regulations).
• This position is eligible for a discretionary bonus and equity award.
Apply Now🕒 July 2
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