Senior Director responsible for evaluating preclinical opportunities in neuroscience at Lundbeck. Engaging with the Boston biotech ecosystem to identify high - impact collaboration opportunities.
About the role
- Senior Director leading clinical trials and development strategies for early oncology assets in a hybrid role. Overseeing projects across hematologic malignancies and solid tumors with cross-functional collaboration.
Responsibilities
- Support clinical trials and the development strategy for early development assets
- Develop clinical development plan from pre-IND stage to first in human clinical trial to proof-of-concept
- Ensure the clinical components of the clinical plans and clinical expertise are provided to project teams
- Support projects from Research to Proof of Concept
- Lead, develop and execute strategic development for early development assets in hematologic malignancies and solid tumors
- Oversee early development assets’ development broadly within a specific indication or group of indications
- Work across the organization and on multifunctional teams responsible for the development of early development assets
- Oversee the development and management of clinical protocols and amendments, investigator brochures, clinical study reports, statistical analysis plan, and regulatory documents
- Provide leadership to early stage clinical scientists on the clinical study team
- Meet regularly with the Pfizer Oncology group leaders/surrogates across functions to increase mutual awareness and influence of emerging program targets, priorities and status
- Drive innovations in early clinical development, and the application of translational oncology and precision medicine approaches.
Requirements
- MD or MD-PhD with 5+ years of industry experience in oncology
- Experience in antibody drug conjugates preferred
- Significant industry leadership experience in clinical, translational or basic research in biomedical sciences or one of the disciplines related to drug development
- Understanding of related disciplines (e.g., biostatistics, regulatory, pre-clinical pharmacology, pharmaceutical sciences)
- Demonstrated scientific productivity (publications, abstracts, etc.)
- Proven scientific writing skills and good communication skills
- Proven leadership skills with ability to defend the clinical plan at governance meetings is essential
- Capacity to adapt to a fast-paced and changing environment
- Demonstrated history of effective leadership; including cross functional and matrixed teams, managing direct reports, and experience in seeking and maintaining alignment with cross-functional leaders
- Demonstrates a passion for helping patients with cancer and for the science of oncology.
Benefits
- 401(k) plan with Pfizer Matching Contributions
- Additional Pfizer Retirement Savings Contribution
- Paid vacation
- Holiday and personal days
- Paid caregiver/parental and medical leave
- Health benefits to include medical, prescription drug, dental and vision coverage
- Eligibility to participate in Pfizer’s Global Performance Plan with a bonus target of 25.0% of the base salary
- Eligibility to participate in share based long term incentive program
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