Tasks & Responsibilities:
- Perform and maintain Drug Demand Planning for Clinical Trials in Phase I, II, and III
- Set-up and maintain Interactive Response Technology (IRT) for multinational Clinical Trials in Phase I, II, and III
- Set-up and maintain clinical trial supply strategy, including set-up of required distribution services and temperature monitoring system for Clinical Trials in Phase I, II, and III
- Establishing, optimization, standardization and harmonization of clinical supply processes and documentation (including SOPs)across multiple clinical trials with very high complexity
- Representing IMP Management team in internal and external project and study teams, organize and facilitate meetings
Requirements:
- Completed studies in the scientific-pharmaceutical or logistic-commercial area or comparable qualification
- Several years of professional experience in the pharmaceutical industry or biotechnology with proven track record of clinical supply chain, logistics set up & management in clinical trials (Phase I, II, III)
- Several years of proven track record of leading setup of IRT systems and temperature monitoring processes in clinical trials
- Sound knowledge and experience in relevant legislation and international GMP, GDP and GCP guidelines
- Effective stakeholder management, both in cross-functional internal and external matrix team environment
- Willing and ready to take over responsibility. Able to rapidly enter in action and to work under stress conditions in a very volatile and agile environment. Intercultural competence and independent, result orientated and proactive way of working
- Excellent organization and communication skills as well as highly motivated and open-minded team player
