Clinical Science Lead m/f/d

At Bayer we're visionaries, driven to solve the world's toughest challenges and striving for a world where ,Health for all, Hunger for none' is nolonger a dream, but a real possibility. We're doing it with energy, curiosity and sheer dedication, always learning from unique perspectives ofthose around us, expanding our thinking, growing our capabilities and redefining 'impossible'. There are so many reasons to join us. If you'rehungry to build a varied and meaningful career in a community of brilliant and diverse minds to make a real difference, there's only one choice.

As a Clinical Scientist Lead (m/f/d), you will be a key figure in leading the clinical science perspective within global oncology development programs. You will create significant impact by safeguarding the quality and integrity of oncology studies and related medical data, optimizing decision-making, and enhancing drug development within a trial's framework. Assigned to highly complex and strategic priority clinical studies, you will provide scientific leadership to develop innovative protocol and study designs, ensuring a scientifically sound end-to-end study strategy.

YOUR TASKS AND RESPONSIBILITIES

• 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

WHO YOU ARE

• 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