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Principal Research Scientist II, siRNA
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AbbVie

Principal Research Scientist II, siRNA

Onsite Worcester, MA, United States Full Time
Posted 17 hours ago
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powertofly approved What AbbVie Has to Offer:

Our work can—and does—have a tangible, lasting impact on millions of people. But it’s not just the results that matter. How we achieve them matters, too. Leading with purpose, we work to build a more sustainable future for generations to come. We do that by putting our expertise, resources and talent to work to make a real difference for patients, communities and our world.

Job Details


Company Description

About AbbVie

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube.


Job Description

The Biotherapeutic and Genetic Medicine (BGM) team at AbbVie is seeking an accomplished Principal Research Scientist to lead the overall strategy for a group and multi-disciplinary project teams. In this role, you will establish a high-throughput siRNA screening platform, drive pipeline innovation through next-generation delivery modalities, and deliver therapeutic leads across multiple disease areas.

Responsibilities:

  • Strategy: Define and drive the multi-year roadmap for the siRNA screening platform, ensuring alignment with therapeutic goals in neuroscience, oncology, and immunology. Collaborate with key stakeholders to balance resources between “platform-building” and “pipeline-driving.”
  • Execution: Oversee the transition of manual assays into robust, automated high-throughput screening (HTS) workflows to identify high-potency siRNA leads. Act as the primary contact between Discovery and Development Sciences (DMPK, Tox, and CMC) to ensure seamless molecule transition and scale-up readiness.
  • Innovation: Design and evaluate next-gen delivery modalities, specifically Antibody, Oligonucleotide Conjugates (AOCs) and tissue-specific ligand conjugates, utilizing advanced chemical modification patterns. Establish “fast-fail” in vivo screening models to rapidly validate functional siRNA delivery to extrahepatic tissues.
  • Leadership: Build, lead and develop a high-performing team of ~ 10 scientists, fostering a culture that is collaborative, agile, and courageous while managing laboratory infrastructure to maximize throughput.

Qualifications

  • BS, MS, or PhD in Molecular Biology, Biochemistry, Chemistry, or a related field with typically 8+ (PhD), 14+ (MS), or 16+ (BS) years of industry experience in biotech or pharma, and at least 5 years in a leadership/management role.
  • Proven track record in siRNA design and the application of chemical modifications for stability and hands-on experience with automation platforms and HTS data analysis.
  • Previous experience leading siRNA platform or portfolio programs targeting tissues beyond the liver is strictly required.
  • Demonstrated ability to advise discipline experts and functional leaders on identifying and mitigating technical and strategic risks.
  • Exceptional interpersonal skills with a proven ability to maintain productive working relationships with diverse internal teams and external collaborators.
  • A strong track record of presenting complex scientific data to internal and external stakeholders.

Additional Information

Applicable 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 program. ​

  • This job is eligible to participate in our long-term incentive program. ​

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. ​

 

AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled. 

US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html

US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:

https://www.abbvie.com/join-us/reasonable-accommodations.html

Company Details
AbbVie
 Chicago, IL, United States
Work at AbbVie

Together, we break through We believe the paths we take to achieving our breakthroughs matter. At AbbVie, every one of our 50,000 employees is a... Read more

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