Join Syneos Health as a Clinical Research Associate II, where your expertise in monitoring and site management will drive successful outcomes in clinical trials. This role requires strong compliance knowledge and offers a team-oriented environment. As an experienced Clinical Research Associate II at Syneos Health, you will conduct site qualifications, monitor adherence to protocols, and ensure data integrity.

Your responsibilities will include evaluating site performance, verifying informed consent documentation, and supporting project objectives through effective communication. You will navigate various tasks while ensuring regulatory compliance and maintaining a focus on patient safety. Key Responsibilities:

- Perform site qualification and monitoring visits both on-site and remotely




- Verify informed consent documentation and patient confidentiality
- Utilize data capture tools and resolve queries effectively
- Maintain accurate Investigator Site File and Trial Master File documentation
- Support patient recruitment and retention strategies

Requirements:

- Bachelor’s degree or RN in a related field
- 12 months of clinical monitoring experience
- Knowledge of ICH/GCP Guidelines and regulations
- Strong computer proficiency and communication skills
- Ability to travel up to 75% regularly

Make a significant impact on clinical research by bringing your monitoring expertise to Syneos Health.

📌 Clinical Research Associate II at Syneos Health (Toronto)
🏢 Syneos Health
📍 Toronto