Назад
Company hidden
7 дней назад

Senior Legal Counsel, Clinical

Формат работы
hybrid
Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
US
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
Для мэтча и отклика нужен Plus

Мэтч & Сопровод

Для мэтча с этой вакансией нужен Plus

Описание вакансии

Текст:
/
TL;DR
Senior Legal Counsel, Clinical (Biotech/AI): Drafting, negotiating, and executing high-volume clinical research agreements to support the development of AI-designed medicines with an accent on clinical contracting, regulatory compliance, intellectual property, and data rights. Focus on managing complex global trial transactions, streamlining study start-up through contracting playbooks, and embedding AI technologies into clinical legal operations.

Location: Cambridge, Massachusetts, United States; hybrid work with office attendance required 3 days per week

Company

hirify.global develops AI models and computational biology technologies to accelerate drug discovery and create innovative medicines.

What you will do

  • Draft, review, negotiate, and execute clinical research agreements, including clinical trial, investigator, site, laboratory, clinical supply, and patient-related agreements.
  • Act as the primary legal partner for the Clinical Development team.
  • Develop and optimise clinical contracting playbooks and template libraries to accelerate study start-up.
  • Identify and mitigate legal, regulatory, intellectual property, data privacy, and compliance risks across global clinical operations.
  • Partner with IP, Corporate Legal, Privacy, and Business Operations colleagues on trial governance and data rights.
  • Manage outside counsel, the clinical transactions legal budget, and the adoption of AI technologies in clinical contracting.

Requirements

  • J.D. or equivalent law degree with active U.S. state bar admission, including Massachusetts Bar admission or eligibility for in-house registration in Massachusetts.
  • Substantial experience structuring, drafting, and negotiating complex clinical trial and related life sciences agreements.
  • Experience in a biotechnology or pharmaceutical legal department or a specialised life sciences law firm.
  • Expert knowledge of clinical trial execution, CRO outsourcing models, and GCP/ICH regulatory guidelines.
  • Ability to manage a high volume of transactions autonomously in a fast-paced environment.
  • Experience with global clinical trial contracting across US, UK, and EU frameworks, including clinical data rights and IP provisions for computational biology or AI platforms.

Culture & Benefits

  • Hybrid working model with in-person collaboration and office attendance three days per week.
  • Collaborative, interdisciplinary environment spanning legal, scientific, medical, and clinical operations teams.
  • Culture guided by thoughtfulness, bravery, determination, and collaboration.
  • Supportive environment focused on shared learning, inclusion, and equal employment opportunities.

Будьте осторожны: если работодатель просит войти в их систему, используя iCloud/Google, прислать код/пароль, запустить код/ПО, не делайте этого - это мошенники. Обязательно жмите "Пожаловаться" или пишите в поддержку. Подробнее в гайде →