8 дней назад
Director, Clinical Supply Chain Operations (Biotech)
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Director, Clinical Supply Chain Operations (Biotech): Developing and managing global clinical supply strategies covering demand planning, packaging, labeling, distribution, logistics, and vendor operations with an accent on clinical trial supply continuity, regulatory readiness, and cross-functional execution. Focus on designing contingency plans, managing global inventory and import/export logistics, leading supplier governance, and driving digital transformation with forecasting tools and AI-driven analytics.
Location: Hybrid role based out of the Bridgewater, New Jersey office, with remote work available most of the time and in-person collaboration as needed. Occasional domestic and international travel of approximately 25% is required.
Company
is a global biopharmaceutical company developing treatments for patients with serious and rare diseases.
What you will do
- Develop and execute global clinical supply strategies, including demand and production planning, packaging, labeling, distribution, returns, reconciliation, destruction, and logistics.
- Define sourcing strategies and manage relationships with CMOs, CROs, 3PLs, IXRS/IRT vendors, and other external providers.
- Establish KPIs, scorecards, governance frameworks, budgets, forecasts, and supplier performance reviews.
- Translate clinical protocols into supply plans, contingency strategies, and risk mitigation across global markets.
- Lead and mentor Clinical Supply managers, build high-performing cross-functional teams, and collaborate with Clinical Operations, CMC, Quality, Regulatory, and Commercial Supply.
- Oversee depot inventory, labeling, temperature excursions, import/export logistics, supply tracking, audit readiness, and patient supply continuity.
Requirements
- Bachelor’s degree in science, business, or a related field.
- 10+ years of experience leading clinical supply chain and logistics activities.
- Extensive experience planning and executing investigational materials supply strategies.
- Expert knowledge of drug development phases, biopharmaceutical processes, and project management principles.
- Experience working across Clinical, Regulatory, and Quality functions in a highly matrixed environment.
- Ability to lead teams, manage cross-functional resources, support regulatory filings, and maintain inspection and audit readiness.
Nice to have
- Master’s degree or MBA.
- Experience in drug development.
Culture & Benefits
- Flexible work schedules with purposeful in-person collaboration.
- Medical, dental, vision, and mental health coverage.
- Paid time off, fertility and family-forming benefits, and caregiver support.
- 401(k) plan with company match, equity awards, ESPP, and company-paid life and disability insurance.
- Learning programs, mentorship, employee resource groups, and service 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 →
Похожие вакансии
10 дней назад
Director, Clinical Supply Chain (Biopharma)
205 000 - 235 000$
13 дней назад
Drug Supply Manager (Pharmaceutical)
8 дней назад
Supplier Governance Senior Manager (Clinical Trials)
13 дней назад
Associate Director, Supply Chain Operations (Pharmaceutical Supply Chain)
167 000 - 206 000$
9 дней назад
Senior Director of Procurement
13 дней назад
Director, Delivery Operations Solutions
150 000 - 216 666$