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The Clinical Research Coordinator is accountable for the planning, preparation, and execution of clinical trials in conjunction with the Team Leader, Project Manager, and Investigator. This role ensures that clinical studies are conducted according to the study protocol, ICH GCP guidelines, and unit SOPs. The coordinator assists in the conduct of Phase I-III studies across all therapeutic areas, ensuring studies are prepared to the highest standard within specified timelines. The role also involves clinical conduct oversight, data cleaning, and deviations management.
Key Accountabilities:
Technical supervision of Clinical Research Nurse, assigned to the studies
Control and direct activities and staff during key operational aspects of assigned studies
Organization and Preparation of clinical studies, as listed below:
Study Protocol review ...