Job Description
Drive clinical research excellence with Syneos Health as an Experienced Clinical Research Associate in a remote setting. Oversee site activities, ensuring compliance and supporting project goals throughout the study lifecycle.
In this pivotal role, you will manage various phases of clinical research, performing site qualification, interim monitoring, and close-out visits. Your expertise in Good Clinical Practice and regulatory standards is essential for safeguarding patient data and safety. Collaborate with a dynamic team to address site-related issues and develop effective action plans for study success.
Key Responsibilities:
- Perform site qualification and initiation visits remotely or on-site
- Ensure compliance with ICH-GCP and protocol requirements
- Manage site monitoring and assessment activities
- Document site activities and maintain required tracking systems
- Serve as a primary liaison with study site personnel
Requirements
- Bachelor’s degree or RN in related field
- Deep understanding of ICH/GCP Guidelines
- Proficient in computer skills and new technologies
- Strong communication and interpersonal abilities
- Willingness to travel up to 75%
Utilize your clinical expertise with Syneos Health to optimize research processes and ensure regulatory compliance effectively.
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About Syneos Health, Inc.
Syneos Health, Inc.
syneoshealth.com
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