Clinical Research Associate

2 weeks ago


Ho Chi Minh City, Ho Chi Minh, Vietnam IQVIA Full time

Responsibilities:

  • Provide monitoring visits and site management for a variety of protocols, sites and therapeutic areas.
  • Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues. Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.
  • Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support startup phase.
  • Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating followup letters and other required study documentation.
  • Build awareness of features and opportunities of study to site.
  • Collaborate and liaise with study team members for project execution support as appropriate.

Requirements:

  • Bachelor's degree in a health care or other scientific discipline or educational equivalent.
  • Minimum of 1+ years of onsite monitoring experience; or equivalent combination of education, training and experience.
  • Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer
  • Good written and verbal communication skills
  • Good organizational and problemsolving skills
  • Effective time management skills


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