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5 дней назад

Associate Clinical Supply Manager (Pharmaceutical R&D)

Тип работы
fulltime
Грейд
senior
Английский
c1
Страна
US/China
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

Текст:
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TL;DR
Associate Clinical Supply Manager (Pharmaceutical R&D): Managing clinical trial packaging, kickoff, import, and delivery activities in China with an accent on GMP/GCP compliance, cross-functional coordination, and supply readiness. Focus on optimizing local packaging processes, mitigating supply risks, supporting health authority inspections, and maintaining reliable clinical supply operations.

Location: North Chicago, Illinois, United States; Conditions: Shanghai, China

Company

hirify.global discovers and delivers medicines and healthcare solutions across immunology, oncology, neuroscience, and aesthetics.

What you will do

  • Manage clinical supply packaging activities with China-based contract pharmaceutical organizations and internal support functions.
  • Coordinate China clinical supply kickoff meetings and align cross-functional teams for study start-up and investigational product readiness.
  • Manage investigational product import and delivery for clinical trials in China.
  • Optimize local packaging processes with external vendors and internal stakeholders to improve efficiency and turnaround times.
  • Support China Health Authority inspections and create or update clinical supply SOPs and work instructions.
  • Maintain reliable investigational product delivery, dispensing, and destruction across clinical sites and depots.

Requirements

  • Bachelor’s degree or above and at least 6 years of experience in pharmaceutical R&D, including at least 4 years in clinical supply chain, CMC, or clinical operations.
  • Knowledge of GMP, GCP, GTC, and clinical supply operations in China.
  • Experience working with contract pharmaceutical organizations in China.
  • Fluent spoken and written Chinese and English required.
  • Strong risk identification, problem-solving, prioritization, communication, and cross-functional collaboration skills.
  • Ability to work independently while ensuring timely, compliant, budget-conscious, and high-quality supply delivery.

Culture & Benefits

  • Work aligned with pharmaceutical quality standards, local regulations, Good Clinical Practices, ICH Guidelines, and company SOPs.
  • Collaborate with global and local clinical operations, quality, regulatory, and supply chain stakeholders.
  • Contribute to innovative medicines and solutions addressing serious health challenges.

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