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2 дня назад

Director, Corporate Counsel (Biotech)

242 000 - 282 000$
Формат работы
remote (только USA)
Тип работы
fulltime
Грейд
director
Английский
b2
Страна
US
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

Текст:
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TL;DR
Director, Corporate Counsel (Biotech): Drafting, negotiating, and managing clinical trial, manufacturing, supply, vendor, and strategic technology agreements with an accent on transactional counseling, risk allocation, regulatory compliance, and intellectual property. Focus on supporting clinical and manufacturing stakeholders, structuring complex biopharma contracts, managing disputes and outside counsel, and improving the contract lifecycle management system.

Location: Remote within the United States; approximately 5% travel.

Base salary: $242,000–$282,000 per year, depending on location, experience, skills, and qualifications.

Company

hirify.global is a late-stage biotechnology company developing durable, disease-targeted gene therapies, including 4D-150 for retinal vascular diseases and 4D-710 for cystic fibrosis.

What you will do

  • Draft, review, negotiate, and execute clinical trial, clinical site, investigator, CRO, vendor, CDMO, supply, manufacturing, quality, material transfer, and technology transfer agreements.
  • Advise Clinical Science, Clinical Operations, CMC, Technical Operations, Supply Chain, Medical Affairs, and other stakeholders on transactional matters.
  • Review clinical trial documents and provide legal guidance on informed consent forms, authorizations, indemnification, and related materials.
  • Advise on contractual risk allocation, indemnification, liability limits, intellectual property ownership, data rights, confidentiality, and regulatory compliance.
  • Support legal policies, templates, playbooks, contract lifecycle management improvements, and the use of outside counsel.
  • Provide counsel on external-facing materials and outreach initiatives, including legal risk mitigation.

Requirements

  • JD degree or equivalent from an accredited law school.
  • Admission to and good standing with at least one U.S. state bar; California admission is preferred but not required.
  • 8+ years of attorney experience, including 5+ years of in-house experience in the life sciences industry.
  • Experience counseling clinical and manufacturing teams and negotiating biopharma agreements under tight timelines.
  • Knowledge of FDA regulations, ICH Guidelines, GxPs, FDCA, FCPA, FCA, AKS, HIPAA, and data privacy laws.
  • Strong analytical, drafting, judgment, problem-solving, collaboration, and workload-management skills.

Nice to have

  • BSc in molecular biology, genetics, biochemistry, or a related biological field.
  • In-house experience at a publicly traded biotechnology, pharmaceutical, or biopharmaceutical company.
  • Large law firm experience supporting life sciences companies.
  • Experience with global registrational clinical trials, intellectual property and technology transactions, commercial disputes, finance teams, auditors, and contract lifecycle tools.

Culture & Benefits

  • Collaborative, service-oriented partnership with cross-functional clinical, manufacturing, supply chain, medical, finance, and management stakeholders.
  • Dynamic, fast-paced environment with autonomous decision-making and aggressive timelines.
  • Sedentary office-style working conditions with no substantial exposure to adverse environmental conditions.
  • Equal employment opportunities and a commitment to a discrimination-free workplace.

Hiring process

  • The role reports directly to the Executive Director, Corporate Counsel.
  • Recruitment agency inquiries are handled exclusively through the internal Talent Acquisition team; unsolicited resumes are not accepted.

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