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10 дней назад

Senior Laboratory Project Services Coordinator (Clinical Research)

Формат работы
onsite
Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
Singapore
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
Senior Laboratory Project Services Coordinator (Clinical Research): Coordinating laboratory activities across clinical studies, including study setup, site loading, investigator portal access, kit shipments, monitoring, and closeout, with an accent on protocol-specific requirements, centralized laboratory monitoring, and stakeholder communication. Focus on identifying performance trends, resolving study issues and escalations, supporting audits and training, and improving laboratory processes and documentation.

Location: Singapore

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, laboratory instructions, monitoring plans, and reports.
  • Coordinate study activities including site loading, investigator portal access, kit shipments, daily performance monitoring, and laboratory centralized monitoring.
  • Manage queries, protocol questions, issues, and escalations with internal and external stakeholders.
  • Review study outputs and reports to identify trends and provide feedback on investigator site and service performance.
  • Coordinate customer communications, project launch meetings, training sessions, audits, inspections, and investigator or client meetings.
  • Contribute to process improvement projects, SOP revisions, document quality control, and junior staff mentoring.

Requirements

  • Bachelor’s degree in life sciences or a related field, or an equivalent combination of education, training, and experience.
  • 1–3 years of relevant experience, preferably in clinical, medical, or healthcare environments.
  • Proficiency in Mandarin is required due to the global portfolio.
  • Good command of English is required for written and verbal communication.
  • Strong interpersonal, communication, organizational, time management, critical thinking, and problem-solving skills.
  • Computer proficiency in word processing, presentation, and spreadsheet applications, with the ability to manage competing priorities in a fast-paced environment.

Culture & Benefits

  • Work across internal and external teams supporting global clinical studies.
  • Opportunities to participate in internal and external meetings, audits, inspections, and training activities.
  • Involvement in process improvement initiatives and SOP development.
  • Work aligned with organizational standards, protocol requirements, and customer expectations.

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