5 дней назад
Senior Associate SP&L (Clinical Supply)
100 960 - 151 440$
Мэтч & Сопровод
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Описание вакансии
Текст:
TL;DR
Senior Associate SP&L (Clinical Supply): Supporting clinical supply planning and execution, including vendor sourcing, packaging and labeling, inventory forecasting, IRT processes, and timely site shipments with an accent on regulatory compliance, patient safety, and cross-functional coordination. Focus on managing drug supply risks, resolving import and export issues, and maintaining accurate distribution and inventory controls across clinical studies.
Location: Basking Ridge, New Jersey, United States
Salary: USD 100,960–151,440 per year
Company
is a global pharmaceutical company developing innovative therapies in oncology, cardiovascular disease, rare diseases, and immune disorders.
What you will do
- Support outsourcing activities, including requirements submission, RFP preparation, proposal reviews, vendor selection, and work-order implementation.
- Coordinate packaging design, patient kit supply preparation, label generation and approvals with vendors.
- Support comparator sourcing, vendor and sponsor discussions, risk identification, and ongoing clinical study activities.
- Help ensure timely site shipments and confirm that clinical materials are released before shipment.
- Support IRT design and processes for drug dispensing, inventory management, forecasting, and distribution.
- Identify issues affecting patient dosing or safety and support resolution of regulatory, import, export, and shipment risks.
Requirements
- Bachelor’s degree in Pharmacy or a related field preferred.
- Four or more years of related experience preferred.
- Experience in project management, clinical supply management, and/or clinical trial coordination required.
- Knowledge of inventory management, drug-supply forecasting and distribution, vendor management, and budget control.
- Experience with IRT or IXRS systems and clinical supply processes.
- Knowledge of GMP, GCP, quality assurance, global regulatory requirements, and import/export considerations.
Nice to have
- PharmD or master’s degree.
- Experience with comparator sourcing, RFPs, and work-order management.
Culture & Benefits
- Work within a global pharmaceutical organization with a focus on innovative medicines.
- Collaborate with cross-functional and international teams.
- Participate in projects spanning clinical trials, supply planning, manufacturing, and regulatory compliance.
- Full-time employment with benefits provided by .
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