Archiviertes Projekt - Clinical Trial Manager (m/f/d)

Ihre Aufgaben:
• Support all project management activities for data generation projects as assigned
• Operationalize data generation projects in close collaboration with the Program Lead: Review committee coordination, contracting, study management team formation, publication support, filing, milestones and budget
• Provide regular updates to internal clinical trial management system for departmental projects, and compile reports from the system
• Support the Associate Director Medical Research Operations Study Management with tracking and update of the medical dashboard
• Act as a key point of contact between Medical Research Operations group and the external research stakeholders and partners

Ihre Qualifikationen:
• Minimum of a Bachelor’s degree in a health-related field with clinical research experience. Master’s degree preferred
• Languages: Written and verbal English required, additional languages advantageous
• Clinical research experience with minimum of 5+ years of CRO/Sponsor Project Management
• Strong Project Management skills including risk assessment and contingency planning; demonstrated learning agility
• Possess a combination of critical thinking and operational know-how and efficiency
• Demonstrated success in working independently
• High level of customer orientation, awareness and focus; strong team leadership skills
• Preference for experience with late phase, post-market, and observational clinical research
• Neuroscience or rare disease experience preferred
• Exceptional analytical, problem-solving, and troubleshooting abilities; strong written and verbal communication skills

Ihre Vorteile:
• International pharma company
• Home office possible

Projektdauer: 4 MM+





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