Principal Scientist, in vivo Pharmacology
Deep Genomics
- Cambridge, MA
- Permanent
- Full-time
- Lead all in vivo work from design, model development, execution, analysis and interpretation.
- Collaborate closely with the therapeutic program teams on relevant in vitro models and development of translational assays.
- Collaborate closely with the target discovery team on availability, feasibility and predictive power of pre-clinical models for new targets.
- Provide strategic leadership on the clinical development path including regulatory filings and biomarker development.
- Demonstrate strong leadership, personal accountability and interpersonal skills, and capability for mentoring (direct reports and others).
- Analyze, interpret and present data to scientists and management in internal and external venues and publish in peer-reviewed journals as appropriate.
- PhD in biological sciences with 6+ years of post-graduate experience in relevant roles (or equivalent) in translational biology for the development of genetic medicines.
- 3+ years building, managing, and leading teams to meet corporate goals.
- Direct experience with pre-clinical models of liver disease.
- Direct experience with LNP or GalNAc-mediated delivery.
- Familiarity with NGS datastreams and interpretation.
- Prior experience executing studies with contract research organizations.
- Breadth of therapeutic area expertise and exposure to multiple therapeutic modalities, ideally including gene editing and RNA-targeted therapies.
- Proven ability to work independently and cross-functionally in a fast-paced environment.
- Strong personal qualities, including attention to detail, emotional intelligence, integrity, creativity, and a willingness to have ideas challenged by team members and to challenge them.
- Ability to communicate complex data sets to key stakeholders from diverse backgrounds.
- Experience with oligonucleotide or gene editing based therapeutics.
- Experience with advanced in vitro models e.g. iPSC derived cells, organoids.
- Experience planning and writing regulatory packages including IND submissions.
- Experience with clinical biomarker development strategy.
- Understanding of target discovery via human genetics.
- Network of relevant external KOLs.
- Strong computational background or demonstrated ability to interface with computational biology teams.
- Experience with multi-site project management and team leadership.
- A collaborative and innovative environment at the frontier of computational biology, machine learning, and drug discovery.
- Highly competitive compensation, including meaningful stock ownership.
- Comprehensive benefits - including health, vision, and dental coverage for employees and families, employee and family assistance program.
- Flexible work environment - including flexible hours, extended long weekends, holiday shutdown, unlimited personal days.
- Maternity and parental leave top-up coverage, as well as new parent paid time off.
- Focus on learning and growth for all employees - learning and development budget & lunch and learns.
- Facilities located in the heart of Toronto - the epicenter of machine learning and AI research and development, and in Kendall Square, Cambridge, Mass. - a global center of biotechnology and life sciences.