Principal Research Associate, Pharmacology

nChroma Bio is a clinical-stage genetic medicines company developing engineered epigenetic silencers to overcome the limitations of existing therapies and enable next-generation genomic medicines. By combining in vivo delivery and gene-regulating technologies, nChroma is designing optimal solutions to deliver precise, potent and durable treatments for patients with high unmet needs. nChroma’s lead candidate, CRMA-1001, is a clinical-stage, liver-directed epigenetic silencer in development as a potential functional cure for chronic hepatitis

B. Guided by a world-class team at the forefront of genetic medicine, founded by renowned pioneers in the field, and supported by top-tier investors, nChroma is redefining targeted in vivo genetic medicine with the initial goal of treating diseases affecting the liver, blood, cardiovascular and central nervous systems.

We’re building a culture and organization to support this important mission, bringing together individuals that thrive in a supportive environment where diverse perspectives and a passion for discovery drive cutting-edge science and breakthrough medicines.

This position will conduct in vivo study work in rodents to support research programs. Perform high level tasks and play a lead role in the day-to-day technical operations as needed. Collaborate with the veterinary staff to ensure that the health and welfare of laboratory animals are maintained in compliance with local, state, federal, and institutional guidelines and regulations.

• Independently perform all procedures and conduct all study types while fulfilling all proficiency standards and expectations.
• Possess strong technical and hands on experience to perform a broad range of in vivo procedures, including common techniques, specialized techniques, and survival surgeries, e.g., dosing, blood collection, necropsy, biomaterial implantations, perfusions.
• Help to manage aspects of technical services, including the day-to-day activities.
• Assist in mentoring, training, and competency/proficiency assessment of laboratory staff.
• Contribute to the development efforts for new in vivo techniques and expand technical service offerings.
• Lead coordination of laboratory projects and initiatives, like audits, supplies/technical equipment management (including routine maintenance), and others.
• Perform study preparation activities, including but not limited to, IACUC and study protocol review, collection tube labeling, and room setup.
• Conduct laboratory procedures in compliance with approved IACUC protocols and study plans. Comply with all SOPs, BOPs, and CRADL standards pertaining to laboratory animals for research.
• Identify and report any experimental/study problems, proactively troubleshoot causative factors, and implement necessary corrections following discussion with supervisor.
• Participate in the development of organizational and function-specific SOPs, in compliance with all state, federal, and industry requirements.
• Document experimental data as requested by clients in technical notebooks or approved electronic files.
• Maintain accurate and up-to-date laboratory records/documentation while assuring quality and data integrity.
• Contribute to IACUC documentation and amendment submissions when required.
• Learn and grow both in technical skills and scientific knowledge base.
• Help management to identify potential problems in the laboratory and think outside the box to make suggestions to improve existing techniques and processes.
• Report non-compliance or animal welfare concerns to the appropriate Animal Welfare Team member or IACUC office.
• Collaborate with other personnel within and across teams and departments to facilitate completion of assignments.
• Ensure that clean work areas and laboratory supply inventory is maintained.
• Attend and participate in on-the-job and classroom training sessions; complete all assigned computer-based safety and professional development training.
• Maintain required attendance level and adherence to work schedule in accordance with required staffing levels to ensure that assigned duties are completed.
• Perform other duties as directed by management.

• Working knowledge and general understanding of the following guidelines and regulations: "The Guide", PHS Policy, and AVMA and importance of ethical use of animals in research.
• Ability to perform effectively under conditions of fluctuating workloads and prioritize job duties with minimal guidance.
• Strong proficiency of in vivo technical skills and comprehensive hands-on experience with mice and rat species, ability to identify sick animals and summarize findings.
• Knowledge and understanding of a variety of animal models in pharmacokinetics, toxicology, oncology, metabolic diseases, infectious diseases, and immune disorders.
• Demonstrate a high level of initiative to troubleshoot and solve issues in the laboratory.
• Strong written and verbal communication skills and ability to work effectively, independently, and…