About this role
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 Degree in a health/life science-related field with initial industry experience in a pharmaceutical/biotech business; 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 Advanced degree in health/life science-related field with a minimum of 1-2 years of industry experience in a pharmaceutical/biotech business; Oncology experience.
About Bayer
Global life science company with pharmaceuticals, consumer health, and crop science divisions. Headquartered in Leverkusen, Germany.