Enhance clinical research integrity as a proactive Clinical Research Associate. Drive compliance and data accuracy while fostering solid relationships with site teams in a flexible setting.In this essential role, you'll be responsible for performing comprehensive site management and monitoring tasks to guarantee adherence to clinical study protocols. Your focus will include evaluating site performance, ensuring informed consent processes are appropriately followed, and documenting key activities. Your impact is vital in maintaining the quality and integrity of clinical trials.Key Responsibilities:
Conduct monitoring visits and site assessments
Ensure proper documentation and tracking of trial activities




Collaborate with site staff for compliance training
Monitor investigational product handling and safety
Prepare for audits and support readiness initiativesRequirements:
Bachelor’s degree or equivalent in a related field
Understanding of Positive Clinical Practice regulations
Strong analytical and computer skills
Excellent interpersonal and communication abilities
Capacity for travel up to 75%Leverage your expertise to maintain the highest standards of clinical research and compliance across trials.#J-18808-Ljbffr

📌 Clinical Research Associate Ensuring Quality Monitoring And Compliance Toronto (Canada)
🏢 Syneos Health
📍 Canada