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 are an excellent communicator and collaborator, able to work effectively with Clinical Operations, Regulatory, Biostatistics, KOLs, and other stakeholders. 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 lead the design and implementation of clinical trial protocols, ensuring adherence to ICH-GCP, ethical standards, and regulatory requirements. * You will provide medical supervision of ongoing trials, working closely with Clinical Operations and ...
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