Principal Scientist, in vivo Pharmacology
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Key Responsibilities
- 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.
Basic Qualifications
- 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.
Preferred Qualifications
- 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.
What we offer
- 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.
This job is no longer accepting applications
See open jobs at Deep Genomics.See open jobs similar to "Principal Scientist, in vivo Pharmacology" Work In Tech.