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As a Clinical Research Associate, you will monitor clinical trial sites, preparing reports and managing monitoring visits while ensuring compliance with regulations.

Freelance coordinator responsible for participant-facing tasks: onboarding, screening calls, follow-up, data collection and tracking, managing in-person processes, reporting AEs/SAEs, escalating issues, and supporting clinical operations.

The Senior Biostatistician will lead statistical strategy and analysis for clinical trials, provide mentorship, and communicate findings effectively.

The Participant Recruitment Coordinator manages participant interactions for clinical trials, ensures data accuracy, conducts onboarding and follow-up, and collaborates with clinical operations to enhance participant experience.

The Configuration Specialist will set up clinical trials on the Citrus platform, ensure compliance, coordinate testing, and manage updates while maintaining data accuracy in a fast-paced environment.