Clinical Research Associate Site Monitor

3 days ago

canada Parexel Full-time $110,000

Clinical site monitoring expertise drives this remote Clinical Research Associate position at Parexel, supporting study quality, patient protection, and site relationships.

As a Clinical Research Associate, you will manage assigned sites from identification through close-out. You will serve as the sites’ sole contact, resolve questions, and oversee delivery. The work includes qualification, initiation, monitoring, and termination visits, alongside report generation and document verification.

Key Responsibilities:

  • Conduct qualification, initiation, monitoring, and termination visits
  • Generate visit and contact reports for assigned clinical sites
  • Build site relationships and resolve study issues
  • Safeguard human subjects’ rights and well-being
  • Evaluate reported data, site efficacy, and drug accountability

Requirements:

  • At least 18 months’ direct onsite monitoring experience
  • Bachelor’s or equivalent degree in a health-related discipline
  • Strong interpersonal, written, and verbal communication skills
  • Knowledge of CTMS, EDMS, Excel, and Word
  • Ability to manage multiple tasks and timelines independently

Apply clinical monitoring, communication, and quality expertise to support compliant research sites and patients through Parexel studies.

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