About Stoke:
Stoke Therapeutics (Nasdaq: STOK), is a biotechnology company dedicated to restoring protein expression by harnessing the body’s potential with RNA medicine. Using Stoke’s proprietary TANGO (Targeted Augmentation of Nuclear Gene Output) approach, Stoke is developing antisense oligonucleotides (ASOs) to selectively restore naturally-occurring protein levels. Stoke’s first medicine in development, zorevunersen, has demonstrated the potential for disease modification in patients with Dravet syndrome and is currently being evaluated in a Phase 3 study. Stoke’s initial focus are diseases of the central nervous system and the eye that are caused by a loss of ~50% of normal protein levels (haploinsufficiency). Proof of concept has been demonstrated in other organs, tissues, and systems, supporting broad potential for Stoke’s proprietary approach. Stoke is headquartered in Bedford, Massachusetts. For more information, visit https://www.stoketherapeutics.com/
Position Purpose:
Stoke Therapeutics is seeking a highly skilled and enthusiastic Senior Research Associate in In Vivo Pharmacology to join our preclinical research team. This individual will be instrumental in the execution of in vivo studies in a fast-paced and exciting environment working with rodent models in the CNS and other therapeutic programs. This position will report to the Associate Director of In Vivo Strategy and Operations.
Key Responsibilities:
• Work cross-functionally with scientists to help design and execute complex in vivo rodent studies to advance Stoke’s preclinical pipeline using antisense oligonucleotides to restore protein expression.
• Perform hands-on rodent procedures including bolus ICV and IT injections in both neonate and adult mice and rats. Other routes of injections include subcutaneous and intravenous injections with subsequent blood collection, serial sampling, and tissue collections.
• Perform adult surgical procedures including dosing, anesthesia monitoring and pre/post-op preparations.
• Execute dose-response, time-course, PK/PD, tolerability and efficacy studies.
• Maintain breeding colonies, wean and genotype, and utilize Softmouse to help expand colonies for experiments.
• Assess animal phenotypes by implementing various behavioral assays like Open Field, DigiGait, and Rotarod.
• With a keen eye for attention to detail, prepare tubes for sample collections and perform necropsies and subsequent tissue homogenization and molecular biology assays.
• Help analyze and interpret experimental data using appropriate statistical approaches and software.
• Maintain accurate laboratory records, electronic notebooks, study protocols, and data reports.
• Other tasks as assigned
Required Skills & Experience:
• S. with 4 years of experience or M.S. with 2 years of experience (relevant industry experience is a plus). Degrees in Pharmacology, Neuroscience or relevant disciplines highly preferred.
• Proficient in various routes of dose administration in mice and rats including, but not limited to, SC, IV, IT and ICV.
• Experience with PK/PD studies in rodents
• Serial sampling in rodents is a plus
• Extensive knowledge of rodent anatomy to perform large scale necropsies
• Experience with anesthesia and pre- and post-op monitoring
• Skilled in surgical techniques such as stereotaxic ICV injections
• Knowledge with rodent behavioral studies of the CNS
• Experience with breeding and colony management
• Tissue processing and homogenization
• qPCR, ELISA, MSD
• Familiarity with Softmouse colony management Software is a plus
• Proficient with Excel, GraphPad Prism, and PowerPoint for data interpretation and presentation
• Electronic Notebook
• Familiarity with writing technical reports
• Strong aptitude for adapting technological advances in the field
Location(s):
Stoke is located in Bedford, MA, and will be moving to a new location in Waltham, MA by the end of 2026. This position is a lab-based position currently in the Bedford office and will later be based in Waltham.
Travel:
This position will require approximately 5% travel.
Compensation & Benefits:
At Stoke Therapeutics, we are committed to offering a comprehensive, competitive and thoughtfully designed total rewards program.
The anticipated salary range for this role is $98,000 - $110,000. The final offer will be determined based on a variety of factors, including role scope, experience and qualifications, education, market benchmarks, internal equity, and geographic location. In addition to base salary, Stoke offers an annual bonus and equity participation.
Our benefits package includes medical, dental and vision insurance; life, long- and short-term disability insurance; paid parental leave; a 401K plan with company match, unlimited vacation time, tuition assistance and participation in our Employee Stock Purchase Program (ESPP). Culture & Values:
At Stoke, we believe that innovation, the ability to successfully advance our ground-breaking science and having fun as a team are enhanced by being together in person, at least periodically. We allow for flexibility in work arrangements that balance individual’s needs and preferences with the needs of our business and our desire to foster a culture of collaboration and innovation.
Our values guide our work to deliver meaningful medicines for people who need them. We are committed to being true to ourselves, to our colleagues, and to the people with severe diseases who are counting on us. We embrace diversity within a unique culture that is defined by our values. Our employee-led Diversity, Inclusion, and Belonging (DIB) Committee underscores the importance of DIB to who we are and what we do.
Interested candidates: Please visit Stoke’s website to learn more and apply directly to the position listed on our Career Center:
https://www.stoketherapeutics.com/careers/
For more information, visit https://www.stoketherapeutics.com/.
All applicants will receive consideration for employment without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, physical or mental disability or protected veteran status.
Stoke participates in E-Verify.