Ihre Aufgaben und Verantwortlichkeiten

• Act as the scientific leader and primary clinical-science representative for assigned global programs
• Perform scientific oversight of oncology clinical trials, ensuring scientific integrity from concept to final report
• Plan and execute data-driven decision-making focused on patient centricity, urgency, and speed
• Lead the development and writing of protocols and related documents, providing training with additional support
• Provide expert input for clinical sections of study reports and assist in regulatory submissions
• Manage studies and provide scientific input to operational colleagues, external parties, and study site staff
• Mentor and onboard junior colleagues, fostering a culture of innovation and collaboration
• Promote creative collaboration between clinicians and scientists to drive the development of a robust pipeline

Wer Sie sind

• Degree in a health/life science-related field with initial industry experience in a pharmaceutical/biotech business; oncology experience is a plus
• Outstanding drug development expertise with knowledge of various diseases and therapeutic areas
• In-depth knowledge of GCP/ICH, FDA, EMA, and relevant regulatory guidelines
• High energy, self-motivated, and proactive with a solution-oriented approach
• Focused on outcomes, independently defining and delivering on high-impact results
• Strong collaborator who encourages open discussion and values diverse perspectives
• Fluent in English; command of a second major European language, especially German, is an asset