Dedicated Clinical Research Associate Comprehensive Site Management

Position: Dedicated Clinical Research Associate for Comprehensive Site Management
Support impactful clinical studies as a committed Clinical Research Associate. Manage site activities, uphold compliance standards, and enhance patient data integrity in a hybrid work model.
This position is integral in conducting site qualification, initiation, and monitoring while ensuring strict adherence to GCP and other regulatory guidelines. You'll collaborate closely with site staff to facilitate data accuracy and effectively manage compliance across trial phases.

Key Responsibilities:

• Lead site qualification, initiation, and close-out activities

• Ensure informed consent processes are thoroughly documented

• Analyze site sources for accurate clinical data

• Oversee investigational products and their compliance

• Engage in subject recruitment and awareness strategies
Requirements:

• Bachelor’s degree or RN in relevant field

• Strong understanding of GCP and regulatory practices

• Excellent communication and tech-savvy skills

• Up to 75% travel requirement

• Ability to adapt to varying project dynamics
Leverage your clinical acumen to optimize site management and bolster data integrity, driving trials to success while fostering patient trust.
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