Associate Director, Clinical Supply Project Manager - Program (Clinical Supply)
Контакты
142 400 - 224 100$
Формат работы
hybrid
Тип работы
fulltime
Грейд
director
Английский
b2
Страна
US
data analysisproject managementgcpsupply chainsapgmpdemand planningclinical developmentclinical supply planning
Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
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Зарплата и рынок
$142к-224к/год
$180к$190кмедиана$220к
По похожим ролям (50) ~ $190к/год
86
Хорошая вакансия
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Роль четко очерчена и предполагает значительную ответственность за программы клинических поставок в крупной биофармацевтической компании; требования и обязанности описаны конкретно.
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Понятная зона ответственностиКрупная фармкомпанияВысокий порог опыта
Оценка от Hirify AI
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Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
Associate Director, Clinical Supply Project Manager - Program (Clinical Supply): Developing strategic and operational plans for end-to-end clinical supply activities across assigned clinical programs with an accent on supply forecasting, bulk drug allocation, timelines, and cross-functional coordination. Focus on managing supply risks, budgets, SAP-based planning, clinical supply documentation, and data-driven decisions across pharmaceutical development programs.
Location: Hybrid, USA - Pennsylvania - West Point. The role is for residents of the United States, Canada, and Puerto Rico. No relocation; travel requirements are 10%.
Salary: $142,400–$224,100 annual base salary, plus eligibility for annual bonus and long-term incentive where applicable.
Company
hirify.global develops pharmaceutical products and manages clinical development programs through its Global Clinical Supply organization.
What you will do
Represent Global Clinical Supply Planning as the primary program-level contact for internal and external customers and lead GCS participation in clinical and development meetings.
Design strategic and operational plans for clinical supply activities across assigned compounds and programs, including bulk manufacturing timelines and drug product release.
Build consolidated product forecasts in SAP and oversee bulk drug supply management and allocation across clinical studies.
Identify and escalate clinical supply risks, manage supply issues, and support program budgets and protocol and program cost estimates.
Mentor new team members, contribute to metrics and cross-functional projects, and drive continuous improvement in planning processes and systems.
Requirements
Bachelor’s degree in a scientific, business, or related discipline is required. An MS or MBA is preferred.
At least 8 years of experience in project management, clinical supply planning, scheduling, coordination and processing of supply chain activities, pharmaceutical development, clinical operations, or related biopharmaceutical functions.
Strong communication, interpersonal, negotiation, influencing, and relationship-building skills for collaboration with cross-functional teams, senior management, external vendors, and clinical sites.
Strong knowledge of project management principles and clinical customer relationship management.
Familiarity with supply chain systems and software such as SAP or Oracle, demand planning principles, and Microsoft Excel, PowerPoint, and Word.
Strong analytical and problem-solving skills, including the ability to analyze complex data, identify trends, and make data-driven decisions.
Ability to adapt to a fast-paced, dynamic environment, manage complex activities, multitask, prioritize work, meet tight deadlines, and maintain strong attention to detail.
Proactive continuous improvement mindset and a proven record in project or portfolio management.
Ability to solve unstructured problems, make informed technical and business risk decisions, balance strategy with tactical execution, and demonstrate ownership and accountability.
Nice to have
Knowledge of Good Manufacturing Practices and Good Clinical Practices.
Experience with ERP systems such as SAP, demand planning tools, and inventory management systems.
Familiarity with data analytics and visualization software.
Familiarity with GMP requirements, quality procedures, and Standard Operating Procedure execution.
Culture & Benefits
Hybrid work arrangement with first-shift daytime hours.
Medical, dental, vision, and other insurance benefits for employees and families.
Retirement benefits including a 401(k), paid holidays, vacation, and compassionate and sick days.
Work focused on customers and patients, ethical decision-making, integrity, collaboration, and continuous improvement.
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