Site Management Associate (Clinical Trial)

PSI CRO AG · Bangkok, Thailand · full-time · Hybrid · yesterday

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Posted October 13, 2026 · Read from PSI CRO
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Job Description

Join our international team and be the key support to clinical research projects, streamlining communication, maintaining systems and managing documents & information.

The scope of responsibilities will include:

  • Maintenance of databases and tracking systems.
  • Serves as the primary sites’ contact point for vendors, study supplies, and access management.
  • Work with large amount of documents, including their compiling, procurement, processing and filing.
  • Communication with company departments and external parties.
  • Communication point for investigative sites participating in the clinical research projects.
  • Coordination of site-specific query resolution, project training and access to vendor-related systems for site teams.
  • Ensures proper administration of sites and vendors payments.
  • Receiving and routing all mails and incoming calls.
  • Assistance with meeting arrangements.
  • Preparation of draft agendas and minutes of project meetings.

Qualifications

  • College/University Degree (Life Sciences)
  • Prior administrative experience in Clinical Research / CRO environment, preferably in an international setting.
  • Good organizational and planning skills, problem-solving abilities, flexibility.
  • Detail-oriented, able to multi-task and work effectively in a fast-paced environment.
  • Team-oriented with excellent customer service and interpersonal skills, including a positive attitude to tasks and projects.
  • Ability to speak Thai and English.
Employer
PSI CRO AG
Location
Bangkok, Thailand · Hybrid
Contract
full-time