About Us Deep Genomics is at the forefront of using artificial intelligence to transform drug discovery. Our proprietary AI platform decodes the complexity of RNA biology to identify novel drug targets, mechanisms, and therapeutics inaccessible through traditional methods. With expertise spanning machine learning, bioinformatics, data science, engineering, and drug development, our multidisciplinary team in Toronto and Cambridge, MA is revolutionizing how new medicines are created. Opportunity The Associate Director, in vitro pharmacology will be responsible for leading the target validation function at Deep Genomics with the goal of advancing our RNA editing therapeutics portfolio. This is a leadership role with the opportunity to make a significant impact on Deep Genomics’ therapeutic pipeline. Success in this role requires the ability to lead strategically, execute tactically, and influence others in a highly matrixed and multidisciplinary team. The ideal candidate will have direct experience in designing, executing and interpreting target validation studies for a variety of liver disease indications. Deep knowledge of a variety of in vitro liver models, relevant functional assays and genome engineering methods is essential. Direct experience with ADAR or other oligonucleotide therapeutics is highly beneficial as is experience with pooled screening approaches and laboratory automation. This role requires leadership from the bench as well as experience supervising junior scientists directly and indirectly. In addition to working closely with the therapeutic program teams, the candidate is expected to work closely with our Target Identification team to translate AI-derived target nominations into a clear action plan leading to go/no-go decisions. As a key member of an early stage discovery team, this individual must demonstrate initiative and ownership in both scientific and strategic decisions and have an entrepreneurial mindset. Ability to pro-actively anticipate needs and independently seek solutions is a key skill, together with effective communication in all directions. This role may lead to the opportunity to manage and mentor direct reports in the future. Please note that the title is commensurate with prior experience. \n Key
Responsibilities Lead all aspects of liver biology target validation from strategy, execution and interpretation, working with direct and indirect reports. Serve as the senior liver biology subject matter expert, leading in vitro pharmacology strategy and collaborating closely with the in vivo pharmacology team to advance therapeutic programs. Collaborate closely with the Target Identification team on availability, feasibility and predictive power of in vitro models and assays for new targets. Present clear, data-driven go/no-go decisions on novel targets. 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 in vitro pharmacology for the development of genetic medicines. 3+ years building, managing, and leading teams to meet therapeutic program goals. Direct, hands-on experience with in vitro models of liver disease and a wide array of functional assays including steatosis, inflammation and fibrosis. Direct, hands-on experience with gene editing or oligonucleotide therapeutics. Proven ability to work independently and cross-functionally in a fast-paced environment. Ability to communicate complex data sets to key stakeholders from diverse backgrounds. 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. Preferred
Qualifications Experience with advanced in vitro liver models e.g. iPSC derived cells, organoids, co-culture systems. Prior experience executing studies with contract research organizations. Experience planning and writing regulatory packages including IND submissions. Understanding of target discovery via human genetics. Strong computational background or demonstrated ability to interface with computational biology teams 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. \n Deep Genomics encourages applications from all backgrounds who seek the opportunity to build the world's leading AI-driven genetic medicine company. If you have a disability or special need, accommodation is available on request for candidates taking part in all aspects of the selection process. *This posting reflects a current vacancy. We offer competitive
compensation aligned with local market benchmarks. The salary range for this role is $195,000 - $230,000, and reflects Cambridge, USA-based roles;
compensation may differ for Canada-based candidates.
