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Clinical science lead m/f/d

Lörrach
Bayer
Inserat online seit: 12 Mai
Beschreibung

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 no longer a dream, but a real possibility. We’re doing it with energy, curiosity and sheer dedication, always learning from unique perspectives of those around us, expanding our thinking, growing our capabilities and redefining ‘impossible’. There are so many reasons to join us. If you’re hungry 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.

Clinical Science Lead m/f/d

As a Clinical Scientist Lead (m/f/d), you will play a pivotal role in leading the clinical science perspective within global oncology development programs. You will safeguard 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

1. Act as the scientific leader and primary clinical-science representative for assigned global programs
2. Perform scientific oversight of oncology clinical trials, ensuring scientific integrity from concept to final report
3. Plan and execute data-driven decision-making focused on patient centricity, urgency, and speed
4. Independently lead the development and writing of protocols and related documents, teaching others as needed
5. May assist in IND (investigational new drug) and NDA (new drug application) submission processes
6. Implement advanced methods of clinical trial design and data generation across the pipeline
7. Provide expert input for clinical sections of study reports and assist in regulatory submissions
8. Serve as a key contact for clinical issues and aspects of assigned studies, ensuring GCP compliance
9. Mentor and onboard junior colleagues, fostering a culture of ownership, innovation and collaboration
10. May co-lead the Early Clinical Team (ECT)

WHO YOU ARE

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

We are looking forward to receiving your application by 28th May. Thank you!

#LI-CH

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