Job description

Requirements

  • Entry level
  • No Education
  • Salary CHF80,000.00 - CHF100,000.00 gross per year
  • Lausanne

Description

The company is a consulting firm.


- Work in close collaboration with other Translational Medicine functions and the Clinical Research Development teams to characterize the pharmacological properties of drug candidates
- Accountable for designing and outsourcing (CROs or academic labs) the pharmacology studies, as well as analysing and reporting the results for a variety of oncology projects
- In vitro/in vivo compounds selection and profiling, including off target characterization, mechanism of action, In vivo proof of concept- PK/PD
- Identification, method development/validation of clinical PD biomarkers
- Contribute to preparation of the pharmacology sections of regulatory documentation (IDB, summaries for IND and IMPD, briefing documentation)
- Define and manage the clinical PD studies (eg blood and tissue biomarkers), incl. data analysis and reporting according to GCP and GCLP
- Support the IP department by contributing to the scientific sections of patent applications
- Contribute to in/out licensing activities for the assets of the company
- Evaluate the pharmacology package of new opportunities and may interact with potential licensees


- PhD in relevant expertise area or equivalent in biomedical engineering
- Profound experience in drug development
- Good understanding of related disciplines including histopathology, bioanalytics, PK and PK/PD
- First Pharma, Biotech or CRO experience
- Fluent in English

  • economists and finance