Job DescriptionAt AbbVie, we are dedicated to addressing the world's most complex and serious diseases. Within the Biotherapeutics and Genetic Medicine (BGM) organization, the newly established siRNA team is building and advancing therapeutic programs from early discovery through development, applying rigorous biology, innovative experimental approaches, and data-driven decision-making to deliver differentiated RNA medicines.
AbbVie is seeking a highly talented and motivated
Senior Scientist I to join our siRNA therapeutics team within BGM at the South San Francisco (ABA) site. The successful candidate will lead in vitro discovery biology efforts to support the development of innovative siRNA-based medicines for oncology. This individual will design and execute experiments, drive scientific innovation, collaborate across multidisciplinary teams, and contribute to advancing therapeutic candidates from early discovery through development candidate nomination for oncology programs. The ideal candidate will possess deep expertise in RNA interference (RNAi) biology and a passion for translating cutting-edge science into transformative medicines.
Responsibilities - Lead and execute in vitro siRNA discovery and proof-of-concept activities, including target validation, assay development and optimization, siRNA screening, lead optimization, and mechanism-of-action studies to support active therapeutic programs for oncology.
- Develop, validate and execute robust siRNA-based in vitro screening funnels for hit-to-lead identification to support siRNA-based drug discovery projects (e.g. 96 well RNA isolation, qPCR, westerns, ELISA, flow cytometry, reporter assays, RNA-seq, microscopy and others)
- Identify and resolve key biological and technical pitfalls related to siRNA activity, delivery, stability, and on-target and off-target effects.
- Maintain updated and well-organized ELNs and ensure high scientific rigor, reproducibility, and data integrity.
- Author internal technical reports and regulatory documents, and contribute as primary author on conference proceedings, manuscripts, and/or inventor of patents.
Qualifications- BS, MS, or PhD in cell biology, molecular biology, biochemistry, pharmacology or related field with typically 0-3 (PhD), 8+ (MS), or 10+ (BS) years of relevant experience.
- RNA biology/therapeutics industry or postdoctoral experience preferred.
- Strong hands-on experience with molecular biology techniques (e.g. stem-loop RT-qPCR and RT-qPCR), including assay design, optimization, validation, and data interpretation for siRNA quantification and mRNA target knockdown.
- Extensive experience with mammalian cell culture and transfection techniques. Experience working with animal tissues would be a plus.
- Demonstrate ability to learn, understand and master new experimental techniques.
- Strong data analysis and critical thinking abilities.
- Routinely demonstrate scientific initiative and creativity in research or development activities.
- Excellent written and verbal communication skills, attention to detail, multi-tasking and organizational skills, and the ability to collaborate effectively with a team.
- Strong presentation skills with the ability to clearly articulate scientific findings and project updates to project teams, senior leadership, and external stakeholders.
- Highly independent and productive in performing laboratory research or assay development, requiring only minimal direction from or interaction with supervisor.
Desired Qualifications - Familiarity with tumor intrinsic biology and/or immune oncology. Experience working with tumor models would be a plus.
- Experience with extrahepatic oligonucleotide delivery technologies, particularly antibody-oligonucleotide conjugates (AOCs), is highly desirable.
- Strong publication track record.
- Ability to work in fast-paced, collaborative environment.
How To Apply If you are passionate about advancing RNA therapeutics and possess extensive hands-on experience in siRNA therapeutic discovery, we encourage you to apply. Please submit your resume highlighting your direct contributions to siRNA programs.
Additional InformationApplicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:
- The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future.
- We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.
- This job is eligible to participate in our short-term incentive programs.
Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company's sole and absolute discretion, consistent with applicable law.
