We're sorry, the job you are looking for at Daiichi Sankyo Europe on EuroPharmaJobs has expired.
Click here to see more jobs at Daiichi Sankyo Europe .
We still have many live jobs. Click below for similar jobs in:
or go to our job search page.
Performing hands-on PBPK, QSP, and clinical trial simulations on an assigned project. Supporting the development of a team from both a technical and scientific perspective to ensure state-of-the-art mechanistic approaches are applied to optimize drug
Act as a regulatory subject matter expert for ICON. Support initiatives to ensure ICON maintains awareness of new regulatory requirements and opportunities and can deliver services accordingly. Actively contribute to maintaining company awareness of new
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
Leads a team of Clinical Pharmacologist leads, providing strategic direction, leadership, and technical expertise for all aspects of clinical pharmacology studies across the IPSEN portfolio, including small molecules, peptides, and biologics (mAbs, ADCs,
Define and lead the scientific strategy for the therapeutic area, aligned with Evotec’s R&D and business objectives; Identify emerging opportunities based on scientific trends, competitive landscape, and unmet medical needs; Champion the therapeutic