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. * Next to this, you will support the development of scientific publications and presentations, serving as a medical and scientific interface to internal and external , including KOLs. * You bring a strong medical and scientific background in hemato-oncology, with proven experience in clinical trial design, execution, and supervision.
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