The role requires expertise in clinical trial design, medical data interpretation, and regulatory compliance, with a strong focus on patient safety, risk mitigation, and adherence to study protocols. * Assist in the review and interpretation of clinical trial data, ensuring accuracy and relevance. * Knowledge of GCP, ICH guidelines, and regulatory requirements for clinical trials * Ability to interpret clinical trial data, assess safety trends, and make informed medical decisions. * Ability to review and interpret clinical data, protocols, and study reports. * Analytical and critical thinking to assess and interpret clinical data effectively. The Medical Monitor is a key clinical expert responsible for ensuring the medical and scientific integrity of clinical trials, overseeing patient safety, and supporting study teams in protocol execution.
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