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.

Early Clinical Lead (all genders)

YOUR TASKS AND RESPONSIBILITIES

• As ECL, you lead the early clinical team responsible for the early clinical development of drug candidates (until Proof of Concept/PoC)
• Accountable and responsible for coordinating the design, execution and delivery of the early clinical development plan, through PoC as well as the clinical pharmacology plan in partnership with other functions and the Global Clinical Lead (GCL), with input from and consensus with other groups e.g. Research Groups, Early Development, Regulatory Affairs and commercial functions
• Work as an internal expert opinion in Target ID teams or early research teams, providing medical/ clinical expertise in order to identify and assess intended indications, patient(sub)populations and drug targets within the global Bayer strategic frames
• Starting during early preclinical research, you provide early clinical development concepts or plans for the respective milestones and starting prior to PCC, he/she ensures definition of an early clinical development and related clinical pharmacology plan, their milestones and, in particular, go/no go decisions and PoC deliverables which fits to the overall therapeutic area strategy
• Ensure the appropriate inclusion of biomarkers and new clinical methodology/technology in close liaise with partner functions such as Translational Sciences
• Provides the medical/clinical assessment justifying the First-in-Man application for approval by the Joint FiM/Tox Release Conference; responsible for the ongoing benefit/risk assessment from FiM until PoC, based on the thorough clinical understanding of the targeted indication and the medical need, the medical/clinical interpretation of study data, and additional relevant medical and scientific information
• Provide input, final review as well as the clinical approval for clinical documents: e.g. study protocols, investigator brochures (IBs), study reports, statistical analysis plans, publications, clinical sections of IND/CTA submissions
• Provides medical/clinical assessment of in- and out-licensing opportunities of research and development projects

WHO YOU ARE

• M.D. with long term relevant professional and academic experience and at least several years` experience of clinical drug development and/or a relevant therapeutic specialty and/ or in clinical pharmacology
• Track record of designing, executing and delivering excellent, focused clinical development plans and clinical studies to produce both timely and good quality data
• Track record of achievement and innovation in pharmaceutical medicine: demonstrated understanding of the complexities and recent developments in the medical area(s) germane to the TA; understanding of issues related to the design and performance of technologically demanding trials; confident discussing scientific/mechanistic aspects of drug development; demonstrated ability to present clinical data, development plans and strategies clearly and accurately to relevant audiences.
• First years of experience in successful leading and managing cross-functional teams
• Strong situational leadership skills (both interpersonal and organizational) to build high-performance, productive teams in highly matrixed environment as well as strong mentoring and coaching capabilities
• Very good communication, networking, negotiation and collaboration skills to engage all involved stakeholders across all levels, ability to drive & influence decision making across all levels of the organization, strong stakeholder management capabilities as well as strong network outside of Bayer
• Ability to constantly challenge existing paradigms in clinical research and encourage use of breakthrough designs based on an understanding of clinical methods, biomarkers and new technologies (including PK/PD modelling and simulation, physiological measurements, imaging, and biochemical/drug assays).
• Fluency in English is essential. Command of a second major European language, ideally German

LI-DE

YOUR APPLICATION

This is your opportunity to tackle the world’s biggest challenges with us: Maintaining our health, feeding growing populations and slowing the rate of climate change. You have a voice, ideas and perspectives and we want to hear them. Because our success begins with you. Be part of something big. Be Bayer.

Bayer welcomes applications from all individuals, regardless of national origin, gender, age, physical characteristics, social origin, disability, union membership, religion, family status, orientation, gender identity, gender expression or any criterion under applicable law. We are committed to treating all applicants fairly and avoiding

Location:            ​ ​  ​   Germany : Berlin : Berlin || Germany : North Rhine Westfalia : Wuppertal-Aprath ​

​ ​ Division: ​               Pharmaceuticals ​

Reference Code:  820548 ​

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