Associate Clinical Supply Distribution Director (Pharmaceutical Logistics)
Контакты
166 500 - 236 500$
Формат работы
onsite
Тип работы
fulltime
Грейд
director
Английский
b2
Страна
US
supply chaingmpvendor managementcustomsgxptrade compliancepharmaceutical logisticsimport exportcold chain managementclinical supply distribution
Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
Пожаловаться
Зарплата и рынок
Средняя
$167к-237к/год
$180к$190кмедиана$220к
По похожим ролям (50) ~ $190к/год
76
Хорошая вакансия
развернуть
Обязанности и условия описаны достаточно ясно, а зарплата и льготы выглядят весомо. Но середина указанного диапазона ниже рыночной медианы, что снижает привлекательность предложения.
Кликните для подробной информации
Ниже рынкаПонятные задачиХорошие льготыБиотех-сфера
Оценка от Hirify AI
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Подключить Plus
Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
Associate Clinical Supply Distribution Director (Pharmaceutical Logistics): Implementing global logistics and distribution strategies for clinical supplies with an accent on depot networks, international import/export compliance, shipment execution, and vendor oversight. Focus on managing cold-chain distribution, customs documentation, temperature excursions, country requirements, and vendor performance across clinical supply operations.
Location: Alameda, California, United States; primarily office-based
Base salary: $166,500–$236,500 annually, adjusted according to geographic market and experience.
Company
hirify.global is a biotechnology company developing and delivering medicines, with clinical supply operations supporting pharmaceutical and biotech programs.
What you will do
Implement global logistics and distribution strategies for clinical supplies and maintain uninterrupted supply to clinical sites and patients.
Set up depot networks and oversee shipment execution, shipper solutions, transit temperature monitoring, and vendor performance.
Manage site-by-site drug product shipments, import documentation, customs clearances, temperature excursions, returns, destruction, and reconciliation.
Ensure compliance with GxP, GMP, import/export, customs valuation, VAT/tax, dangerous goods, and other trade requirements.
Partner with clinical operations, clinical supply chain project teams, trade compliance specialists, vendors, and industry experts to resolve issues.
Maintain country requirement and distribution databases, support budgets, and improve vendor service through governance models and KPIs.
Requirements
BS/BA degree with at least 11 years of related experience, or MS/MA degree with at least 9 years of related experience, or an equivalent combination.
Technical experience in international pharmaceutical logistics and supply chain, preferably in pharmaceutical or biotech industries.
Strong experience in clinical supply distribution and knowledge of regulations governing clinical supply activities.
Experience with cold-chain management, process optimization, drug product delivery, and temperature-controlled logistics.
Experience with international trade compliance, imports, exports, HTS, country of origin, customs valuations, and dangerous goods requirements.
Strong communication, stakeholder management, collaboration, problem-solving, and staff supervision skills; proficiency with MS Office and specialized applications.
Culture & Benefits
Collaborative office environment focused on sharing ideas and solutions.
Equipment provided, including dual monitors and ergonomic chairs.
401(k) plan with company contributions, medical, dental, vision, life, disability, and flexible spending benefits.
Annual discretionary bonus eligibility and long-term incentive opportunities.
15 vacation days in the first year, 17 paid holidays including a winter shutdown, and up to 10 sick days annually.
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 →