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3 дня назад

Supplier Governance Sr Mgr (Biotech)

134 264 - 181 651$
Формат работы
remote (только USA)
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

Текст:
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TL;DR
Supplier Governance Sr Mgr (Biotech): Overseeing supplier performance and quality for globally sponsored clinical trials with an accent on governance meetings, KPI monitoring, supplier selection, and cross-functional collaboration. Focus on managing supplier issues, improving clinical trial execution, implementing technology and innovation, and leading stakeholder and direct-report development.

Location: United States - Remote

Salary: $134,264.30–$181,651.70 annually

Company

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

What you will do

  • Oversee supplier performance and quality for hirify.global-sponsored global clinical trials.
  • Facilitate supplier governance meetings and operating reviews, monitor KPIs, and manage issues.
  • Support supplier evaluation, selection, onboarding, and startup activities.
  • Align supplier strategies and capabilities with business priorities in collaboration with leadership.
  • Coordinate process improvements, clinical trial execution standards, technology assessments, and cross-functional initiatives.
  • Mentor direct reports and manage performance, feedback, training, and career development.

Requirements

  • Doctorate degree and 2 years of clinical experience; or master's degree and 4 years; bachelor's degree and 6 years; associate's degree and 10 years; or high school diploma/GED and 12 years.
  • Experience in life sciences or a medically related field, including clinical research experience with clinical trials.
  • Experience working with or overseeing clinical trial suppliers, preferably in a biotechnology, pharmaceutical, or CRO environment.
  • Knowledge of Good Clinical Practices, FDA regulations and guidelines, and international regulatory requirements.
  • Experience with clinical trial execution, project management, proactive issue management, and communication with senior management.
  • Strong interpersonal, organizational, supervisory, collaboration, and leadership skills.

Nice to have

  • BS, BA, or BSc in the sciences, or an RN qualification.
  • Experience managing direct reports and working in a global, matrix organization.
  • Experience working for clinical trial suppliers.

Culture & Benefits

  • Collaborative, innovative, and science-based work environment.
  • Health, dental, vision, life, disability, and flexible spending benefits.
  • Retirement and savings plan with company contributions.
  • Annual bonus program, stock-based long-term incentives, and time-off plans.
  • Career development opportunities and flexible work models where applicable.

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