Report to SVP, Head of Oncology Clinical Development and lead clinical development for lung and head/neck cancer portfolio
Accountable for end-to-end clinical development from FTIH through POC, registrational trials, regulatory approval and initial market launch
Ensure medical, clinical and disease area knowledge is integrated into pre-clinical research activities
Lead and drive disease area knowledge and co-lead the Lung Oncology Tumor Team
Lead R&D scientific advisory boards to position individual and portfolio assets
Build and maintain partnerships with Oncology Research Unit, Medical Affairs, Global Product Strategy and external collaborators
Lead intra- and inter-department cross-functional teams, working groups or workstreams
Contribute to establishment of clinical standards and processes within Oncology Clinical Development
Manage, mentor and coach Clinical Development Leads, Clinical Science Program Leads, Clinical Scientists and Medical Directors; allocate resources across portfolio
Provide ongoing coaching, development and leadership including regular staff meetings, check-ins and 1:1s
Guide cross-functional integration, coordination and alignment to enable effective CDP execution
Foster team culture: be bold, be swift, act with integrity, OneOncology community
Position requires on-site presence 2–3 days/week in listed office locations
Requirements
Medical degree and a clinical medical specialty qualification/registration in Internal Medicine, Medical Oncology (adult or peds), Hematology or Pathology
Direct line management experience of oncology clinical development teams
Matrix management experience
Pharmaceutical experience in early and late phase Oncology drug development
Experience with clinical and translational investigation of Oncology agents in lung and head/neck cancers
Experience integrating translational research activities into first-time in human (FTIH) trials to establish clinical proof-of-concept
Experience successfully developing and executing oncology Clinical Development Plans
Experience in the successful filing, approval and initial launch of a novel oncology therapy
Experience working with external scientific experts and clinical key-opinion-leaders and orchestrating scientific advisory boards
Experience working with regulatory agencies and ability to provide clinical leadership for the filing of INDs and NDAs
On-site office-based presence 2 to 3 days a week in specified locations (UK, Switzerland, US or Poland)
Preferred: PhD in addition to medical degree and registration/certification