Over eight years of Clinical Research experience in Global/multinational studies (Phase I, II, III & IV) across on various therapeutic areas in multidisciplinary team.
Responsible for negotiations of clinical trial budgets and study site budget management, updates to sponsor and training to CRA鈥榮 to enhance monitoring skills. Perform as Visit Leader and conduct CRA performance visit for sign off CRA's. Assists Clinical Trial Manager with CTM tasks.
Responsible for clinical trial monitoring and management of site data and activities to provide necessary quality and data required for global regulatory submissions for approval of drugs.
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