Contract Clinical Research Associate

Job Summary

Seeking experienced Contract Clinical Research Associates to monitor studies in Oncology, Cardiology, or Ophthalmology on a contract basis, with a focus on managing clinical trials remotely while being based in PST, MST, or CST time zones.

Key responsibilities

• Monitor clinical studies to ensure compliance with protocols and regulations
• Collaborate with cross-functional teams to support trial execution and data integrity
• Prepare and review study-related documentation and reports

Required qualifications

• Experience in monitoring clinical trials, specifically in Oncology, Cardiology, or Ophthalmology
• Knowledge of Good Clinical Practice (GCP) and regulatory requirements
• Ability to work independently and manage multiple studies simultaneously
• Based in PST, MST, or CST time zones
• Relevant degree in life sciences or a related field