Clinical Research Associate

JOB TYPE: Contract and Full Time
CATEGORY: Pharmaceutical


The Clinical Research Associate (CRA) has responsibilities for the delivery of the studies at allocated centers and are active ensuring that quality and quantity commitments are achieved in a timely and efficient manner.

Major responsibilities:

  • Manage EC submission, Initiation, Monitoring and Closure of clinical studies
  • Proactive to drive recruitment at study sites. Identify study-related issues and escalates to the team to ensure recruitment target is achieved with speed and quality.
  • Obtain and maintain essential documentation, electronic Trial Master File in compliance with ICH-GCP, SOP and local regulations
  • Update relevant systems with data from centers as per required timelines.
  • Manage study drug and study supplies at study sites.
  • Ensure accurate and timely reporting of Serious Adverse Events and other safety report.
  • Prepare for activities associated with audits and regulatory inspections
  • Collaboration with local team to contribute to process improvements, knowledge transfer and best practice sharing.

Minimum Requirements and Preferred Background:

  • Bachelor degree or higher, preferably with a pharmacy, nursing or medical related field
  • 2 -3 years’ experience in clinical trial monitoring
  • Fluent in English and Thai ( verbal and written).
  • Ability to travel nationally as required.
  • Excellent ability to prioritize and handle multiple tasks.
  • Good presentation and communication skills, verbal and written
  • Good project management, analytical, decision-making, organizational and interpersonal skills.
  • Good computer skills and ability to learn and to adapt working with IT systems

Only Thai residents need to apply.

Please fill in the form below to submit your application:

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