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8 часов назад

Sr Associate Project Manager - Remote (Biosimilars)

89 168 - 120 639$
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
Sr Associate Project Manager - Remote (Biosimilars) (project management, analytical similarity): Managing sample workflows and project coordination for biosimilar candidates progressing toward regulatory approval with an accent on inventory planning, laboratory database management, and data verification. Focus on coordinating cross-functional scientific teams, distributing samples for testing, organizing LIMS and ELN data, and ensuring regulatory document accuracy.

Location: United States - Remote

Salary: $89,168.40–$120,639.60 per year

Company

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

What you will do

  • Provide project management for technical teams developing biosimilar candidates through regulatory approval.
  • Manage analytical similarity samples, inventory planning, sample distribution, and incoming project data.
  • Coordinate with Similarity, Critical Reagents, Data Management, and scientific teams.
  • Create electronic laboratory notebooks and manage sample submissions, work orders, and controlled document archives.
  • Query LIMS, ELN, and other databases; organize and retrieve data for review and verification.
  • Verify data in internal and regulatory documents and format materials according to internal standards.

Requirements

  • Master’s degree, or a bachelor’s degree plus 2 years of project management experience.
  • Alternatively, an associate’s degree plus 6 years of project management experience, or a high school diploma/GED plus 8 years of project management experience.
  • Strong analytical, organizational, communication, Microsoft Word, and Microsoft Excel skills.
  • Knowledge of good data practices, data verification, collaboration systems, and document management.
  • Ability to manage multiple priorities and collaborate across scientific and regulatory functions.

Nice to have

  • Experience supporting pharmaceutical research and development or nonclinical drug development programs.
  • Experience with document management systems, collaboration platforms, project management tools, LIMS, or ELN software.
  • Experience coordinating scientific or regulatory documents throughout their lifecycle.
  • Bachelor’s or advanced degree in life sciences, regulatory affairs, business, or a related field.

Culture & Benefits

  • Employee health, dental, vision, life, disability, and flexible spending benefits.
  • Retirement and savings plan with company contributions.
  • Discretionary annual bonus and stock-based long-term incentives.
  • Paid time off and biannual company-wide shutdowns.
  • Career development opportunities and flexible work models where available.

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