Join a leading team as a Clinical Research Associate focusing on site monitoring in a sponsor dedicated capacity. This flexible role allows for both remote and site-based work.
In this position, you will ensure the integrity of clinical trials by conducting comprehensive site assessments, verifying consent processes, and maintaining compliance with applicable regulations. You will be tasked with managing site-level activities, communicating effectively with investigators, and contributing to audit readiness. Your expertise in monitoring processes will play a critical role in the success of clinical projects.
Key Responsibilities:
- Conduct on-site and remote monitoring visits
- Verify accuracy of clinical data and site documentation
- Manage inventory and compliance of investigational products
- Document and communicate site performance issues
- Participate in training and meeting preparations
Requirements:
- Experience in site monitoring and clinical research
- Knowledge of GCP and regulatory compliance
- Strong organizational and communication skills
- Ability to adapt to evolving project demands
- Mentorship experience is a plus
Make a significant contribution to advancing clinical trials and ensuring quality in research activities.
Clinical Research Associate – Monitoring Specialist in Toronto employer: Syneos Health
At Syneos Health Communications, we pride ourselves on being an exceptional employer that fosters a collaborative and innovative work culture. As a Remote Search Media Director, you'll enjoy the flexibility of remote work while being part of a dynamic team dedicated to driving impactful results in the pharma sector. We offer extensive employee growth opportunities, competitive benefits, and a commitment to professional development, making this an ideal place for those seeking meaningful and rewarding careers.
