5 дней назад
Associate Director, Clinical Supply Chain (Oncology)
167 000 - 206 000$
Мэтч & Сопровод
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Описание вакансии
Текст:
TL;DR
Associate Director, Clinical Supply Chain (Oncology): Managing clinical trial materials for precision oncology programs with an accent on forecasting, sourcing, packaging, labeling, distribution, and vendor oversight. Focus on designing supply strategies, monitoring IRT inventory, coordinating global shipments, and maintaining compliant clinical drug supply across Phase 1–3 trials.
Location: South San Francisco, CA; hybrid schedule with onsite work required four days per week. Domestic travel of approximately 5–10% is required.
Salary: $167,000–$206,000 per year.
Company
is a precision medicine oncology company developing targeted therapies, including small-molecule treatments and antibody-drug conjugates, for molecularly defined solid tumors.
What you will do
- Manage clinical trial material supply planning, demand forecasting, inventory monitoring, allocation, distribution, returns, and destruction.
- Coordinate packaging, labeling, expiry extensions, batch records, retain samples, and study-specific pharmacy and training materials.
- Manage external depots, couriers, contract packaging organizations, CMOs, CROs, and other clinical supply vendors.
- Develop and oversee study-specific IRT requirements, user acceptance testing, inventory monitoring, resupply, updates, and issue resolution.
- Prepare and oversee documentation for global shipment, import/export, customs clearance, and compliant delivery to clinical sites.
- Collaborate with CMC, QA, QC, Clinical Operations, Regulatory, and Program Management to mitigate supply risks and support clinical trials.
Requirements
- BA/BS in Supply Chain, Engineering, Life Sciences, or a related field; APICS, CPIM, CIRM, or PMP certification is desirable.
- 10+ years of experience in the biotechnology or pharmaceutical industry, including 7+ years in supply chain.
- Experience managing clinical drug supply for global Phase 1–3 trials, Expanded Access Programs, and investigator-sponsored trials.
- Demonstrated experience with IRT systems, forecasting, inventory management, drug allocation, global labeling, packaging, and over-labeling.
- Experience managing external packaging and distribution partners and supporting international shipments and customs clearance.
- Deep understanding of GMP, GDP, GCP, regulatory timelines, global distribution, logistics, and cross-functional clinical operations.
Nice to have
- Experience with CMC operations and drug supply forecasting technology.
- APICS, CPIM, CIRM, or PMP certification.
Culture & Benefits
- Collaborative, inclusive, and data-driven environment focused on precision oncology and patient outcomes.
- Medical, dental, and vision coverage, with the company paying 100% of employee premiums and 90% of dependent premiums.
- 401(k), employee stock purchase plan, wellness programs, discretionary short-term incentives, and potential stock option awards.
- Work-from-home flexibility within the required hybrid onsite schedule.
- Employees working at company facilities must be fully vaccinated against COVID-19, subject to applicable accommodations and legal requirements.
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