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CRA Trainee

The Programme




  • Conducts monitoring (pre-study, initiation, routine monitoring and closeout visit), if required.Conducts co-monitoring visits, if required
  • Conducts Quality Oversight Visits (QOV), as requested
  • Completes monitoring visit/ QOV reports timely
  • Assists with investigator/site identification
  • Assists site to prepare Ethics Committee submissions
  • Facilitates clinical trial site contract and budget negotiation
  • Manages site queries and communications.Assists in managing clinical trials, if required;
  • Establishes regular lines of communication with sites and COMs
  • Provides protocol and related study training to assigned sites
  • Evaluates the quality and integrity of site practices – escalating quality issues as appropriate
  • Manages site performance by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution

Required Skills and Abilities

  • Bachelor’s level degree or above in life sciences, pharmacy, nursing or medical
  • Understands clinical trial processes with a thorough knowledge of ICH and associated regulatory guidelines
  • Excellent organizational skills and ability to prioritize and multitask
  • Fluent in English (writing and speaking)
Closed a year ago
Closed a year ago
  • Job type:Graduate Jobs
  • Disciplines:

    Science, Pharmaceuticals, Nursing, Medicine

  • Citizenships:

  • Locations:

    Beijing (China)

  • Closing Date:21st Mar 2019, 6:00 pm


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