You will contribute to study design, regulatory submissions, data review, and publications, while collaborating closely with cross-functional teams to maintain the highest standards of patient safety and regulatory . * You will ensure regulatory compliance, providing medical guidance on safety, adverse events, and study conduct, and contributing to the preparation of regulatory submission packages. * In addition, you will work closely with cross-functional teams, including Clinical Operations, Regulatory Affairs, Biostatistics, and external partners, to ensure the smooth execution of clinical programs and foster a culture of scientific excellence and * You have industry experience in Pharma/Biotech, ideally in a cross-functional, global clinical development setting. * You are committe
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