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. * Participate in safety review meetings, data monitoring committees (DMCs), and investigator meetings. * 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.
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