- Supervision of GCLP-compliant immunogenicity testing for clinical trials (scientific, technical and organizational aspects)
- Establish, maintain and supervise collaborations with external partners
- Development and validation of immunological assays
- Writing technical protocols/reports and other GxP documentation as well as support preparation of clinical study documentation
- Provide expertise and support to other functions within the organization
- Evaluation and presentation of data
Requirements
- PhD in the fields of Immunology, Virology and/or Microbiology
- Work experience in the life science industry or experience with clinical studies is a plus
- Hands-on experience on immunological/biological assays/analytical methods (e.g. ELISA, cell based assays, RT-qPCR)
- Knowledge in development of assays
- Experience in an GxP environment is a plus
- Excellent analytical/problem solving skills
- Strong organizational and communication skills
- Fluent English
- Good presentation techniques
- Able and used to work under time pressure on multiple projects in a changing environment
Benefits
- Open, appreciative company culture with innovative spirit and attractive assignments
- International surrounding with flat hierarchies
- Good team spirit in a strong and highly motivated team
- Wide range of benefits
Due to legal reasons we are obliged to disclose the minimum salary for this position, which is 48.000,- gross per year based on full-time employment. However our salaries are market oriented and in line with your qualifications and experience.