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6 дней назад

Lab Project Coordinator (Clinical Research)

Формат работы
onsite
Тип работы
fulltime
Грейд
junior
Английский
b2
Страна
China
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
Lab Project Coordinator (Clinical Research): Supporting the Project Manager and study teams throughout the full clinical study lifecycle with an accent on study setup, laboratory monitoring, stakeholder coordination, and closeout. Focus on overseeing protocol-specific laboratory requirements, resolving study queries and escalations, monitoring site performance, and coordinating customer communications.

Location: Beijing, China

Company

hirify.global provides clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries.

What you will do

  • Support Project Managers with study setup, planning, meeting minutes, action logs, and protocol-specific laboratory instruction documents.
  • Coordinate routine study activities including site loading, Investigator Portal access, kit shipments, and day-to-day performance monitoring.
  • Oversee protocol-specific Laboratory Centralized Monitoring and use reports and monitoring tools to identify trends.
  • Coordinate with internal and external stakeholders to resolve queries, protocol questions, issues, and escalations.
  • Lead customer communications when the Project Manager is absent and oversee project closeout activities.
  • Participate in meetings, audits, inspections, and study training for sites, CRAs, and customers.

Requirements

  • High school diploma or equivalent required; a bachelor's degree in life sciences or a related field is preferred.
  • Relevant clinical, medical, or healthcare experience is preferred; equivalent education, training, and experience may be considered.
  • Good command of English is required; excellent command of the local language is preferred for China-based communication.
  • Strong interpersonal, written and verbal communication, organizational, time management, critical thinking, and problem-solving skills.
  • Ability to manage competing priorities, use resources effectively, comply with applicable standards, and work in a fast-paced environment.
  • Computer proficiency with word processing, presentation, and spreadsheet applications.

Culture & Benefits

  • Work aligned with standard operating procedures, organizational standards, protocol requirements, and customer expectations.
  • Opportunity to collaborate with internal and external teams across clinical research studies.
  • Participation in internal and external meetings, audits, inspections, and training initiatives.
  • Focus on integrity and truthful, complete information throughout the hiring process.

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