Switzerland
Posted 3 years ago
Key responsibilities
- Represent the Pharmacology and Screening function in Clinical Study teams, Translational Medicine, and Global Project Teams
- Design, plan, manage and report microbiology and pharmacology studies:
- In vitro/in vivo compounds selection and profiling, including off target characterization
- Proof of concept in vivo studies – PK/PD
- Mechanism of action and resistance studies
- Identify and lead method development/validation and analyses of clinical isolates and pharmacodynamic clinical biomarkers / Contributes to the development of ASTs in line with EUCAST and CLSI requirements
- Determine, implement, and manage the clinical microbiology analyses, data analyses and reporting according to GCPs and GCLPs
- Manage outsourcing activities to an international network of CROs
- Manage external collaborations with KOLs and universities
- Input the elaboration of the clinical development strategy
- Contribute to the preparation of the pharmacology and clinical documentation required for Health Authorities submissions
- Participate in external scientific communications and represent the organization during international scientific events
- Contribute to in/out licensing activities and internal innovation pipeline
Your profile
- PhD in the field of microbiology
- 5-7 years experience in translational research and antibiotics R&D in pharma or biotech
- Knowledge of GCP and ICH guidelines, animal welfare regulations, and relevant regulatory guidelines
- Excellent communication skills (oral and written) in English
- You are used in working in cross-functional team and fast-paced environment and are a team player, looking to tackle challenges together with your team
- Experience in Oncology would be a plus
Job Features
| Job Category | RESEARCH |