Associate Director, Clinical Scientist Oncology - London

Job summary

This position will require 2 to 3 days per week onsite at a GSK office location. The Associate Director, Clinical Scientist, Oncology has accountability for providing clinical input during protocol development, oversight of study conduct, and interpretation of study results consistent with objectives to define safety, efficacy, pharmacokinetic/pharmacodynamic, and patient reported outcomes, and applicability of data to the targeted patient population.

Responsibilities

• Ensure delivery of quality study strategy and design, understand the analysis and interpretation of data throughout the study
• Lead or contribute, as appropriate, to the end to end (protocol concept to final study report) delivery of clinical development activities which ensure consistency with the clinical development strategy for regulatory approvals, reimbursable medicines, and successful lifecycle management
• Understand the asset's biological mechanism, clinical strategy, scientific interpretation of disease and target-based literature
• Integrate data from internal, and external academic, conference and competitor sources
• Understand and support creation and support of competitor landscape, medical need, regulatory strategy
• Appropriately interact with Key External Experts (KEEs), Key Opinion Leaders (KOLs), collaborators, etc.

Job description