Care Access
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Create, maintain, version-control, and archive eSource and paper source documents for clinical trials per GCP and 21 CFR Part 11. Design templates from protocols/CRFs, coordinate reviews and updates, communicate with site staff and internal teams, and ensure documents capture required trial data.
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Provide medical oversight for clinical trials, ensure participant safety and protocol compliance, perform assessments and study procedures, review safety reports and CRFs, train and support sub-investigators and staff, participate in monitoring/audits, and comply with ICH GCP and regulatory requirements.
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The Digital Marketing Manager will develop and execute digital campaigns to increase patient engagement and recruitment, utilizing analytics for optimization and budget management.
