7 дней назад
Senior Legal Counsel, Clinical
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
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.
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