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Regional Study Coordinator

Singapore, Singapore · Job Posted May 03, 2026
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Job Description

Labcorp is seeking a Regional Study Coordinator to join our team in Singapore.

Job Responsibility

  • Be responsible for managing clinical projects to ensure the successful delivery of all lab services, including kits shipment, sample testing and sample management of a clinical study for the Asia region
  • Act as regional liaison between Labcorp Central Lab Services (CLS) Global Study Manager and various CLS departments involved in the clinical protocol
  • Close collaboration with the Global Study Manager for all study related aspects that are pertaining to the Asia platforms and through all study stages, from set-up to closure
  • Review the study Statement of Work, a document that specifies the scope of services CLS will perform for a clinical protocol and contains information approved by the sponsor and necessary to define the protocol specific database, to ensure regional feasibility and make appropriate recommendations to the Study Design Lead
  • Ensure a detailed knowledge of the Statement of Work specifications and very good understanding of how they impact every lab services aspect of the clinical trial
  • Manage day-to-day regional study related activities, including responding and resolving challenges in logistics, lab tests resulting, monitoring and study supplies, keeping the Global Study Manager informed of any study development
  • Monitor, track and provide resolution to all local study issues, keeping the Global Study Manager in the communication loop
  • Responsible for implementing monitoring and setting up of local performance metrics and taking corrective actions when needed
  • Liaise with the Global Study Manager for any tasks assigned to the Regional Study Coordinator as part of the Global Monitoring Plan
  • Demonstrate ability to work in a matrix environment where task assignments can be channeled down to be completed by Regional Study Coordinators while other task assignments will need to be delegated to other functional groups
  • demonstrate flexibility in handling both categories of tasks
  • Participate in functional meetings, learning forum and provide input, keeping processes up to date
  • Support a culture of continuous improvement, quality and productivity
  • Support CLS Global Project Management strategy and deliver outstanding customer satisfaction and performance

Requirements

  • Bachelor Degree in Life Sciences or Pharmaceuticals
  • 3 months or more experience using computer and office software applications (e.g. Microsoft Word, Excel, MS-Access and Outlook)
  • Professional or internship experience in clinical research or pharmaceutical industry
  • Proficiency in Chinese language as liaising with China counterparts is expected
  • Strong interpersonal skills
  • Influence and negotiation skills
  • Demonstrated ability to plan and prioritize
  • Demonstrated communication and organizational skills
  • Demonstrated attention to detail
  • Demonstrated participation in process improvement initiatives
  • Proven ability to excel in a fast-paced environment
  • Proven teamwork
  • Proven experience and knowledge of processes and tools used in department
  • Demonstrated ability to liaise with internal departments
  • Demonstrated ability to facilitate meetings

Nice to have

  • Professional or internship experience in clinical research or pharmaceutical industry
  • Proficiency in Chinese language as liaising with China counterparts is expected
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