- Design and coordinate studies to understand the potential effects of gene editing products
- Interpret and report data from investigative and translational studies to drive mechanistic understanding
- In partnership with R&D teams, facilitate appropriate incorporation of translational medicine strategies for early and late phases of development
- Implement and coordinate innovative biomarkers for defined endpoints based on the best available science and emerging multi-omic technologies
- Utilizes literature reviews, protocols, networking, and prior laboratory experience to advance the pre-clinical and clinical goals of the organization
- Author research papers, abstracts, technical reports, and sections of regulatory documents
- Effectively present and communicate research findings to internal and external collaborators, including upper management, regulatory agencies, and at research conferences
- Collaborate with internal and external stakeholders
- Other duties within the nonclinical development department, as assigned
- Ph.
- At least 10 years of relevant experience
- Strong hands-on experience with translational lab methodologies (ex. cell-based techniques, ex-vivo drug testing and models, PK/PD assays)
- Ability to collaborate and influence at all levels across an organization
- Exceptional written and verbal communication allowing oneself to communicate scientific data and information to others in a digestible format
- Analytical mindset and good problem-solving ability
- Demonstrated ability to critically evaluate and contribute to multiple scientific programs
- Diligence and attention to detail
- Good organizational skills
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Principal Scientist, Translational Hematology - Boston, United States - Verve Therapeutics Inc
Description
The PositionVerve is looking for a Principal Scientist with expertise in translational biology research, specifically in hematology.
This individual would be responsible for designing translational and investigative research studies to bridge the gap between early research and clinical studies, thereby supporting the strategic development of gene editing based drug products.
This individual will work cross functionally within the nonclinical development team and with the clinical and regulatory teams to provide mechanistic insights and translational capabilities relevant to the development of Verve's gene editing medicines.
Job Responsibilities