Reporting to the of Clinical Operations (EU), the Medical Monitor works closely with , investigators, and internal clinical teams to ensure the highest ethical, medical, and regulatory standards throughout the clinical trial lifecycle. * Collaborate with investigators, , clinical operations teams, and regulatory authorities to support study execution. * Provide medical information to clinical research teams, ensuring alignment on trial protocols and safety procedures. * Previous Medical Research experience(e.g., in CRO, Pharma, Hospital or with a Regulatory Body). * Knowledge of clinical research methodologies, study design, and statistical concepts.
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