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The role will provide scientific and technical leadership for analytical development at various stages of drug development both internal and external through CDMO with particular emphasis on research and early development (pre-DP0) including material
Serve as a clinical and scientific subject-matter expert for the assigned therapeutic area and disease indication, with a strong focus on protocol execution and data integrity; Work cross functionally to ensure clinical strategy is translated into the
This role is accountable for defining the vision, operating model, and multi-year strategy for internal QC to support Genmab’s evolving pipeline and transition to a fully integrated, commercial-stage biotechnology company. The role will shape future QC
Act as the primary point of contact for the client and study team on assigned projects from the initiation through to the close-out of a project. Attend relevant study meetings such as Business Development handover and Kick-Off Meeting along with
The scientific and strategic leader of oncology drug discovery programs, accountable for driving projects from early concept to Preclinical Candidate (PCC) nomination, in alignment with Oncology Therapeutic Area and R&D strategy. As the integrator of