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4 дня назад

Project Svcs Lab QC Analyst

Формат работы
onsite
Тип работы
fulltime
Грейд
middle
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
Project Svcs Lab QC Analyst (Clinical Research Quality Control): Reviewing project databases and requisition forms against sponsor protocols and requirements with an accent on quality standards, clinical research terminology, and audit readiness. Focus on identifying quality trends, resolving findings with project stakeholders, maintaining QC timelines, and improving study set-up processes.

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

  • Perform quality control reviews of project databases and requisition forms against sponsor protocols and requirements.
  • Collaborate with Set-up Managers, Project Managers, and Set-up Coordinators to resolve quality findings and process issues.
  • Maintain adherence to QC timelines and support client delivery needs.
  • Analyze quality trends and identify opportunities for training and process improvement.
  • Coordinate with global QC counterparts to maintain consistency in study set-up processes.
  • Participate in internal and external audits as required and follow ICH E6 Good Clinical Practice guidelines.

Requirements

  • Bachelor’s degree in a science-related field.
  • At least 2 years of clinical or research industry experience, including 1 year in study set-up or project management.
  • Experience demonstrating strong attention to detail, organization, operational skills, and deadline management.
  • Proficiency with Microsoft Office, Q Squared Solutions systems, and ELVIS.
  • Knowledge of medical and clinical research terminology.
  • Good command of English and strong written and verbal communication skills.

Culture & Benefits

  • Full-time position in Beijing, China.
  • Cross-functional collaboration with internal stakeholders and sponsor organizations.
  • Work in a fast-paced, deadline-driven clinical research environment.
  • Collaboration with global QC counterparts to support consistent processes.

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