Our lead candidate, a tandem CAR-T cell product, is currently undergoing pivotal clinical trials on a global scale. You will be responsible for the development and oversight of clinical and regulatory documents that support global drug development programs, including preparation, development, review, revision and finalization of clinical documents for submission to regulatory authorities. * Your responsibility includes ensuring that all documents are scientifically sound, strategically aligned, and compliant with global regulatory standards. * Collaborating closely within cross-functional teams (clinical, regulatory, biostatistics, safety), you drive consistency and alignment across all deliverables and contribute to overall project success. * Your profile is rounded by a solid understanding of drug d
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