Site Management Associate (Clinical Trial)

atPsicro

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.
  • 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.
Skills required
  • Procurement
  • English (Fair)
  • Thai (Fair)
Experience required
  • any or no experience
Salary
  • 22,000 - 36,000 THB, Negotiable
Job function
  • Medical / Health Care
Job type
  • Full-time

Company overview

Size:n/a
Industry:Medical / Pharmaceutical
Location:n/a
Website:www.psi-cro.com
Founded in:n/a

PSI CRO is a full-service contract research organization that runs clinical trials for pharmaceutical and biotechnology companies. It manages studies from start-up and site monitoring through data management and regulatory work.

The company hires clinical research associate ...

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