Dec 22, 2024
Site Name: Cambridge MA, GSK HQ, USA - Pennsylvania - Upper Providence Posted Date: Dec 19 2024 This role within Global Clinical Oncology R&D will serve as a clinical sciences leader on global oncology studies and contribute to program-level activities. Responsible for the delivery of quality study strategy and design, understanding the analysis and interpretation of data throughout the study, including leading clinical data review ongoing throughout study conduct. Responsible for the end to end of writing protocols (protocol concept to final study report) delivery. Contributor to informed consent forms development and other study related documents. Clinical Development Oncology Key Responsibilities: Review and/or enhance the technical and scientific robustness of project level clinical development plans. May support regulatory interactions, including contributing to briefing documents, presentations, addressing questions and responses. Ensure compliance with...
GlaxoSmithKline
Collegeville, PA, USA
Full-Time