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Vice President Early Development Portfolio Lead
Company | Bayer |
Address | Cambridge, MA, United States |
Employment type | FULL_TIME |
Salary | |
Category | Chemical Manufacturing,Biotechnology Research,Pharmaceutical Manufacturing |
Expires | 2023-08-08 |
Posted at | 10 months ago |
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.
- Drives overall R&D assessment and provides medical assessment of in and out-licensing opportunities of development projects;
- Lead cross-functional and functional activities to accelerate drug development and decision making; drive medical value and differentiation generation in target identification efforts ;
- Design a ‘state-of-the-art’ product development strategy for the assigned portfolio area and composing assets based on state-of-the-art science understanding patient, regulatory and commercial needs;
- Ensures timely and transparent and objective communications about program status and issues between IPT and management;
- Constantly reviews the market environment in order to ensure the program’s strategy is meeting patient, regulatory and commercial needs;
- Actively seeks opportunities to represent Bayer in various external forums and panels, such as industry consortia, government-industry panels, professional societies and patient-focused groups;
- Fully responsible as a physician for all medical/clinical aspects for assigned drug candidates until PoC. Accordingly, responsible for the ongoing benefit/risk assessment of drug candidates and for taking relevant actions and decisions as appropriate, based on the thorough medical/clinical understanding;
- Deliver portfolio program milestones in a timely, cost-effective and high-quality fashion from D1 to Proof of Concept. This includes derisking of programs and investments as early as possible;
- Creates and leads motivated, committed and engaged teams. Models and expects effective team behavior to achieve the project goals.
- Oversee development of the Target Product Profile (TPP) and revisions thereof;
- Liaises with Research, Late Development, and Commercial to ensure smooth project transitions through product life-cycle and alignment on the project objectives and deliverables across the portfolio covering multiple MoA across many tumor types;
- Comprehensive knowledge of scientific, development and regulatory landscape to enable state-of-the-art development strategies for all assets;
- Set the vision and strategy for the assigned portfolio areas; will prioritize and make strategy recommendations on assigned portfolio area including on strategic external partnerships for new areas such as novel combinations opportunities and new therapeutic modalities;
- Accountable for driving technical reviews for the programs in the portfolio;
- Networks with Key Opinion Leaders and maintains effective external scientific advisory boards which is especially important for the new and rapidly developing IO territory;
- Exposure to and understanding of commercial considerations in relation to drug development;
- Relevant global health authority interactions and current knowledge of regulatory review and responses;
- Expertise with cancer and non-cancer cell targeted drugs as well as different modalities including small and large molecules;
- The successful candidate will be an PhD, or an MD or an MD/PhD;
- Board certification within oncology/hematology or associated subspecialties;
- Knowledge of the entire R&D process and the key drivers for success as well as strong understanding of the elements of drug development programs;
- Strong consensus-building skills and the ability to lead multidisciplinary teams towards sound decision-making;
- Evidence of ability to lead and manage a team to deliver to time, cost and quality requirements.
- Scientific excellence: Demonstrated by a track record of relevant basic and/or translation research documented in peer reviewed publications;
- Excellent communication and leadership skills, coupled with the ability to develop and implement a strategic growth plan;
- High energy with focus and vision; self-motivated with a high sense of ownership, urgency, proactive and solution-oriented;
- Command of a second major European language, especially German.
- 7+ years of drug development experience with at least 3+ years of expertise in early drug development;
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