Responsibilities

The (Associate) Medical Director will provide medical leadership to study teams, including creating clinical trial protocols and implementing scientific information, contribute to site selection, review and approve study protocols and amendments, Clinical Study Reports (CSRs), Informed Consent Forms (ICFs), Case Report Forms (CRFs), and protocol deviation decisions. They will also monitor clinical studies in real time, ensuring medical validity and subject safety, proactively address customer concerns, and serve as a liaison between sponsors and internal departments. Furthermore, the Medical Director will educate investigator sites through protocol-specific lab procedures presentations and demonstrations during investigator meetings, control and handle daily activities during clinical trials, and serve as a medical point of contact for all stakeholders, including investigators, IRBs, and Health Authorities.