Назад
Company hidden
2 дня назад

Supplier Governance Senior Manager (Clinical Trials)

Формат работы
onsite
Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
US
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
Для мэтча и отклика нужен Plus

Мэтч & Сопровод

Для мэтча с этой вакансией нужен Plus

Описание вакансии

Текст:
/
TL;DR
Supplier Governance Senior Manager (Clinical Trials): Overseeing supplier governance, performance, risk, and quality for Amgen-sponsored clinical trials with an accent on Clinical Pharmacology CROs, laboratory suppliers, and cross-functional collaboration. Focus on supplier evaluation and selection, proactive risk management, process improvement, regulatory compliance, and leading direct reports.

Location: Washington, D.C., United States

Company

hirify.global is a biotechnology company developing, manufacturing, and delivering medicines for serious illnesses across oncology, inflammation, general medicine, and rare disease.

What you will do

  • Facilitate supplier governance meetings, operating reviews, KPI monitoring, and issue management.
  • Support supplier evaluation, selection, onboarding, and startup for clinical trial programs.
  • Develop supplier strategies aligned with business priorities and capabilities.
  • Manage relationships with study teams, functional leads, procurement, quality, compliance, and external suppliers.
  • Lead supplier risk management, process improvement, clinical trial execution standardization, and technology initiatives.
  • Mentor direct reports, manage performance, and contribute to cross-functional projects.

Requirements

  • Degree and clinical experience combination ranging from a doctorate with 2 years to a high school diploma/GED with 12 years of clinical experience.
  • BS/BA/BSc in the sciences or RN qualification.
  • 9 years of experience in life sciences or a medically related field, including 6 years in biopharmaceutical clinical research.
  • Experience with Clinical Pharmacology, laboratories, clinical trial suppliers, risk management, and direct reports.
  • Knowledge of Good Clinical Practices, FDA regulations, and international regulatory requirements.
  • Strong project management, issue management, communication, leadership, organizational, and supervisory skills.

Culture & Benefits

  • Comprehensive employee benefits, including retirement contributions, medical, dental, vision, life, disability, and flexible spending plans.
  • Discretionary annual bonus program and stock-based long-term incentives.
  • Award-winning time-off plans.
  • Flexible work models where applicable to the posted work location type.
  • Collaborative, inclusive, science-based environment with professional development opportunities.

Будьте осторожны: если работодатель просит войти в их систему, используя iCloud/Google, прислать код/пароль, запустить код/ПО, не делайте этого - это мошенники. Обязательно жмите "Пожаловаться" или пишите в поддержку. Подробнее в гайде →