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Driving all aspects of purification process development, characterization, and technology transfer to cGMP manufacturing for hybrid and continuous processes; Serving as an internal technical resource for cGMP manufacturing and Process Design as well as a
Strategic and scientific leader within Clinical Development, driving the advancement of ProQR’s pipeline and contributing to improved patient outcomes. As a subject matter expert in CNS diseases, the Medical Director provides deep scientific and
You’ll be leading a team of Pharmacometricians, from both a technical and scientific perspective, to ensure state of the art pharmacometrics approaches are applied to optimize drug discovery and development. Performing hands-on population PK/PD,
You will provide technical leadership and scientific expertise to support the commercial manufacturing of pharmaceutical products. This role is responsible for ensuring robust process performance, driving continuous improvement, troubleshooting technical
Responsible for the development, maintenance and adherence to Genmab’s clinical data standards including eCRFs, edit checks, electronic case report forms (eCRFs) Completion Guidelines, controlled terminology, CDISC, CDASH and etc. The Associate Director