• Develop and validate bioanalytical in-vitro potency assays
• Responsibility for conduct of pre-clinical studies
• Manage global studies conducted at CROs, overseeing their daily and on-going activities, including interactions with project managers, scientists, statisticians and contract department
• Manage interactions with opinion leaders, advisors, consultants
Qualifications:
• At least 5 years of experience as a scientific project manager at a biotech or pharma company working in international environment
• Documented experience in setting-up and validation of bioanalytical assays
• Ability to lead multiple scientific projects in parallel
• Creative thinking/ problem solving
• Ability to present scientific data at meetings
• Good writing skills
• Excellent communication skills; good working relationships
• Fluent in English
• Background education: Ph. D degree in life sciences