gdprdue diligencecontract negotiationdata privacycontract lifecycle managementhealthcare lawclinical trial agreementspharmaceutical law
Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
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Зарплата и рынок
Средняя
$203к-243к/год
$160к$190кмедиана$240к
По похожим ролям (48) ~ $190к/год
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У роли четкий фокус на уровне senior, зарплата соответствует рыночному ориентиру, а работа с международными онкологическими исследованиями делает вакансию сильной для опытного юриста в фармацевтике.
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Широкий круг договоровЗарплата по рынкуОнкологическая биотехнологияПонятная зона ответственности
Оценка от Hirify AI
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Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
Senior Legal Counsel (Pharmaceutical): Drafting and negotiating clinical collaboration, clinical trial, research, supply, and commercial agreements for a biopharmaceutical oncology company with an accent on clinical development contracts, regulatory compliance, and risk management. Focus on leading complex negotiations, advising cross-functional stakeholders, supervising legal reviews, and supporting acquisition due diligence.
Location: Menlo Park, CA; Miami, FL; Princeton, NJ; or Remote within the United States
Salary: $203,000–$242,563 USD annually, plus potential bonus, stock, benefits, and other variable compensation.
Company
hirify.global is a biopharmaceutical oncology company developing investigational therapies and conducting global Phase 3 clinical studies.
What you will do
Draft, review, and negotiate clinical trial collaboration agreements and related supply, delivery, quality, and clinical services agreements.
Handle clinical trial agreements, investigator-sponsored studies, sponsored research agreements, CRO agreements, and other commercial and operational contracts.
Partner with business development, clinical development, clinical operations, medical affairs, finance, research and development, and other internal functions.
Identify contractual risks, propose practical alternatives, and escalate matters to the Chief Legal Officer or General Counsel when appropriate.
Supervise attorneys and paralegals, prepare contract templates, provide contracting training, and report contract status to internal stakeholders.
Support acquisition and asset-transaction due diligence and handle additional legal assignments.
Requirements
Juris Doctorate and admission to a US state bar in good standing are required.
At least 7 years of major law firm and/or in-house experience with a pharmaceutical, medical device, or healthcare company.
Substantial experience serving as lead attorney for drafting and negotiating Clinical Trial Collaboration Agreements.
Experience drafting and negotiating US and ex-US clinical trial agreements for a pharmaceutical company.
Knowledge of clinical trial, pharmaceutical research, development, commercial contract, data privacy, and GDPR requirements.
Strong legal drafting, analysis, communication, organizational, negotiation, and risk-management skills, with the ability to manage multiple deadlines independently.
Nice to have
Experience with acquisition or divestiture due diligence.
Experience with contract lifecycle management systems and the ability to learn new systems quickly.
Working knowledge of Microsoft Word, Excel, and Teams.
Culture & Benefits
Work within a legal department supporting a growth-stage biopharmaceutical company.
Collaborate with cross-functional teams and external partners on global clinical programs.
Compensation may include bonus, stock, benefits, and other applicable variable compensation.
Work is available from the listed US locations or remotely.
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