5 дней назад
Associate Clinical Supply Manager (Pharmaceutical R&D)
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
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
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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