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Senior Scientist , Pipeline Development & SAR Optimization

Job in Greenlawn, Suffolk County, New York, 11740, USA
Listing for: Allergan
Full Time position
Listed on 2026-02-01
Job specializations:
  • Healthcare
  • Research/Development
    Research Scientist
Job Description & How to Apply Below
Position: Senior Scientist I, Pipeline Development & SAR Optimization
Location: Greenlawn

Company Description

Abb Vie'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 – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about Abb Vie, please visit us at  Follow @abbvie on X, Facebook, Instagram, You Tube, Linked In and Tik Tok.

Job Description

At Abb Vie, we are dedicated to solving some of the world’s most complex and serious diseases. Our mission is to develop and deliver advanced therapeutics that change lives. We are looking for talented, passionate, and driven individuals to join our Biotherapeutics and Genetic Medicine (BGM) team. As a Senior Scientist in our siRNA group, you will be part of an innovative team focused on advancing RNA-based therapies that have the potential to revolutionize patient care.

Abb Vie is looking for a Senior Scientist I to join our siRNA group within the Biotherapeutics and Genetic Medicine (BGM) department. This role will involve designing and executing innovative experimental approaches to address key scientific challenges related to oligonucleotide therapeutics. The successful candidate will drive scientific innovation, identify new methods and techniques, and collaborate across functions to support the development of novel RNA-based therapies.

Responsibilities
  • Lead research efforts within a cross-functional team to advance new therapeutic targets for siRNA-based pipeline development.
  • Design and execute in vitro and in vivo proof-of-concept studies to evaluate siRNA library and characterize lead compounds for the target engagement and therapeutic benefits.
  • Design and execute structure-activity-relationship (SAR) studies for lead optimization, including optimization of siRNA sequence, chemical modification patterns, conjugation sites and linkers, etc.
  • Provide scientific leadership and expertise in candidate nomination and pipeline development.
  • Work independently and maintain a high level of productivity in the laboratory, ensuring efficiency and scientific rigor.
  • Analyze and interpret multidisciplinary data to generate actionable conclusions and guide future experimental directions.
  • Collaborate and effectively communicate results with key stakeholders and cross-functional teams throughout the organization.
  • Contribute as a primary author to scientific publications, presentations, and/or as a primary inventor of patent applications.
  • Mentor and support junior scientists within the team.
Qualifications
  • BS, MS, or PhD in chemistry, molecular biology, biochemistry, or related field with typically 10+ years (BS), 8+ years (MS), or 0-3 years (PhD) of experience.
  • Demonstrated expertise in siRNA therapeutics, including library design, screening and characterization of SAR.
  • Demonstrated expertise for siRNA candidate nomination and pipeline development.
  • Extensive hands-on experience and techniques for molecular and RNA biology, including cell culture, RNA extraction, RNA quantification (RT-PCR, qPCR, ddPCR), next-generation sequencing (NGS) library preparation, protein assays (ELISA, Western Blot, JESS), flow cytometry and other biomarker quantification.
  • Experience in assay development and high-throughput screening for siRNA target identification and validation, mechanism of action studies, biodistribution and biomarker analysis is a plus.
  • Strong understanding of ex-hepatic delivery of siRNA is highly desirable.
  • Proven ability to develop, troubleshoot and refine assays to enhance sensitivity, reproducibility, and throughput.
  • Highly self-motivated and capable of thriving in a fast-paced, collaborative team environment.
  • Strong written and verbal communication skills, with experience contributing to technical reports, publications, or regulatory documentation.
Why Abb Vie?

Abb Vie is a global biopharmaceutical company committed to bringing innovative medicines to patients in need. We offer a collaborative work environment, opportunities for professional growth, and the ability to make an impact on…

Position Requirements
10+ Years work experience
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