CompensationCHF 150,500 - 297,500 annual base salary; performance-based bonus possible.
Requirements2+ yrs exp · PhD · EU/EFTA permit
How you match
01
Skills
02
Clinical trialshealth sciencesClinical trial protocol draftingClinical research operationsPharmaceutical developmentRegulatory Compliance in MedicineGlobal Medical StrategyTechnical decision-making
Languages
English
Compensation
03
CHF 150,500 - 297,500 annual base salary; performance-based bonus possible.
The role
04
01Provides strategic medical and scientific leadership and expertise to all line functions on the project team for the development of new oncology agents.
02Creates clinical development strategies for new oncology agents within the PE/ DC to TDP timeframe.
03Delivers solutions within functions, across functions, and on global projects.
04Leads Biomedical Research Early Program Teams (BPTs) to enable the start of clinical development.
05Collaborates with clinical scientists to develop clinical protocols for TCO compounds.
06Applies own medical knowledge to guide the safe, ethical and efficient conduct of the trials.
07Liaises with outside experts, investigators, and regulatory authorities in oncology.
08Writes and reviews abstracts/manuscripts for presentation/publications.
Requirements
↳Education: MD or DO degree.
↳Board-certification in an oncology specialty and PhD-level science is preferred.
↳A minimum of 2 years of industry experience within pharmaceutical or biotechnology organizations.
↳Experience in the interpretation of preclinical oncology data.
↳Recognized as an expert in your field by external medical experts and regulatory authorities.
↳Excellent interpretation of oncology preclinical data.
↳Strong knowledge of the application of PK/PD and biostatistics to clinical development.
