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5 дней назад

Senior Associate SP&L (Clinical Supply)

100 960 - 151 440$
Формат работы
onsite
Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
US
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

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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

hirify.global 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 hirify.global.

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