Associate Clinical Operation Manager
Valneva, Austria

• Proactive support of all aspects of one or more phase 1-4 clinical studies
• Support in the implementation of clinical studies from start-up to study completion
• Contribution to the development of study relevant documents in the project development cycle
• Support in CRO/vendor selection process and CRO/vendor oversight
• Monitoring and execution of all study activities in compliance with ICH-GCP and FDA/EMA/MHRA requirements
• Cross-functional collaboration with internal and external stakeholders (e.g. CROs)
• Support in budget planning and financial tracking

Requirements

• Academic education, Master or PhD degree (Life Science)
• At least 2 years of relevant experience as a CRA in the pharma/life science industry
• Project management experience is an advantage
• Ideally experience in the field of vaccine development as well as supervision of CROs and CRAs
• Team oriented, stress resistant personality
• Strong communication and organizational skills
• Ability to prioritize and maintain oversight
• Very good command of English (spoken and written)

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 like flexitime, performance-related bonus, lunch vouchers, child care center (Kindergarten), company events

Due to legal reasons we are obliged to disclose the minimum salary for this position, which is 50.000,- gross per year based on full-time employment. However our salaries are market oriented and in line with your qualifications and experience.

Job Rewards and Benefits