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5 дней назад

Sr Lab Project Set-Up Coord

Формат работы
onsite
Тип работы
fulltime
Грейд
senior
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
Sr Lab Project Set-Up Coord (Clinical Trials/Laboratory Databases): Supporting the design, configuration, validation, and documentation of laboratory project databases for clinical studies with an accent on data quality, established procedures, and customer requirements. Focus on coordinating study setup, identifying project risks, maintaining regulatory compliance, and mentoring junior staff.

Location: Beijing, China

Company

Provides clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries.

What you will do

  • Support the design, configuration, loading, and validation of laboratory databases in Clinical Trials Management Systems.
  • Assist with study validation, database design requirements, protocol amendments, and project planning.
  • Research setup issues, coordinate with laboratory colleagues and internal departments, and communicate relevant risks to project stakeholders.
  • Maintain accurate project documentation and contribute to timelines, regulatory steps, internal audits, and process improvement projects.
  • Coordinate planning and handover meetings and communicate factual information with study sponsors.
  • Manage low-complexity study setup activities where applicable, while mentoring and training junior staff.

Requirements

  • High school diploma or equivalent required; a bachelor's degree in life sciences or a related field is preferred.
  • At least 1 year of relevant experience in the clinical, medical, or healthcare industry, or an equivalent combination of education, training, and experience.
  • Strong organizational, coordination, written, and verbal communication skills with a good command of English.
  • Demonstrated quality, accuracy, attention to detail, and ability to work in a fast-paced environment.
  • Computer proficiency in word-processing and spreadsheet applications.
  • Ability to establish effective working relationships with co-workers, managers, clients, and sponsors.

Nice to have

  • Technical and operational knowledge of Clinical Trial Management Systems.
  • Knowledge of laboratory processes and computer systems.
  • Bachelor's degree in life sciences or a related field.

Culture & Benefits

  • Work follows standard operating procedures, company policies, and good practice requirements.
  • Activities are conducted in accordance with the ICH E6 Guideline for Good Clinical Practice.
  • Opportunities to participate in local and global process improvement projects.

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