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The Clinical Research Associate coordinates clinical monitoring and site management processes to ensure trial compliance with protocols, ICH-GCP guidelines, and regulatory standards. They perform risk-based monitoring, data verification, and maintain collaborative relationships with investigative sites to ensure data reliability and subject safety.
The Senior Clinical Research Associate will coordinate clinical monitoring and site management processes to ensure protocol and regulatory compliance. They will also provide mentorship to junior team members and collaborate with cross-functional teams to resolve study issues.
Coordinate day-to-day remote clinical trial operations and facilitate remote patient visits. Manage data entry in EDC and CTMS systems while serving as a virtual liaison between sponsors and CROs.
Provide high-quality mental health support through psychotherapy, counseling, or coaching sessions. Lead support groups and deliver Masterclasses to clients across the Asia-Pacific and Europe regions.
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Serve as the primary operational support for the VP of Operations, managing projects and ensuring deliverables are met. Oversee patient recruitment, contracting, and the design of e-source templates and workflows.
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