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3 дня назад

Clinical Project Manager II (Life Sciences)

74 000 - 93 000$
Формат работы
onsite
Тип работы
fulltime
Грейд
middle
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
Clinical Project Manager II (Life Sciences): Managing clinical and life sciences projects covering sample management, laboratory services, logistics, and regulated products with an accent on client coordination, project planning, regulatory compliance, and delivery tracking. Focus on monitoring schedules and scope, managing quality and risk, resolving queries, and supporting FDA- and GXP-regulated operations.

Location: Plainfield, Indiana, United States; general office setting. Occasional travel of up to 10% may be required, along with work in areas containing potentially infectious materials.

Salary: $74,000–$93,000 per year

Company

hirify.global provides genomic services, automated biosample management, laboratory analysis, informatics software, and sample storage solutions for pharmaceutical, biotech, academic, and healthcare organizations.

What you will do

  • Serve as the primary client contact for assigned clinical and life sciences projects.
  • Create, implement, and maintain project plans while tracking schedules, scope, performance metrics, and deliverables.
  • Coordinate sample management, kit provision, logistics, laboratory services, training, relocation services, and alliance support as required.
  • Document customer expectations and manage delivery in compliance with regulatory requirements.
  • Lead quality assurance, risk management, query resolution, continuous improvement, and SOP development activities.
  • Participate in presales discussions and client meetings, and mentor Client Coordinators as needed.

Requirements

  • Bachelor’s degree in science or a related field and at least 2 years of project management experience, or a high school diploma or equivalent and at least 5 years of project management experience.
  • Experience in FDA- and GXP-regulated environments.
  • Strong organizational skills and attention to detail.
  • Excellent verbal, written, presentation, and problem-solving communication skills.
  • Ability to collaborate, gain commitment, prioritize competing demands, and complete long-range projects.
  • Ability to maintain a clean work environment and follow Universal Precautions for bloodborne pathogens.

Nice to have

  • Master’s degree in science or a related field.
  • CSPO, CSM, or PMP certification.

Culture & Benefits

  • Customer-focused culture centered on innovation, accountability, teamwork, integrity, and employee value.
  • Opportunities to contribute to continuous improvement, quality, productivity, and audit-ready SOP initiatives.
  • Work supports life sciences systems and services used in drug development, clinical trials, and advanced cell therapies.

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