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Translational Research Scientist

Job in Rahway, Union County, New Jersey, 07065, USA
Listing for: AA2IT
Full Time position
Listed on 2026-07-03
Job specializations:
  • Research/Development
    Clinical Research, Research Scientist, Biotech Research, Medical Science
Salary/Wage Range or Industry Benchmark: 53 USD Hourly USD 53.00 HOUR
Job Description & How to Apply Below
Position: Translational Research Scientist - I

Translational Research Scientist

Pay Rate: $53/HR

Education Minimum Requirement:

  • BS in a life sciences discipline (Biochemistry etc.) or Chemistry
  • MS or PhD preferred.

Required

Experience and Skills:

  • A minimum of 7-8 years (BS), 5-6 years (MS) or 3 years (PhD) of pharmaceutical industry experience
  • A minimum of 5 years of direct experience in immunoassay development

Preferred

Experience and Skills:

  • Broad knowledge of drug development process and translational medicine
  • Hand-on experience in clinical development/operation or managing the implementation of biomarker assays in support of drug development
  • Experience with Regulated Clinical bio-analysis

Note:

Onsite lab based role. Positions available:
1. Possibility of extension.

Responsibilities:

  • Utilizing the technologies of Flow Cytometry, Molecular Pathology, Immunochemistry, Mass Spectrometry and Genomics, the Translational Molecular Biomarkers (TMB) is responsible for clinical biomarkers in all therapeutic areas and in all phases of clinical development at Client Research Laboratories. Candidate should have a strong interest in Translational Sciences.
  • Develop and validate immunoassays (ELISA, MSD etc) within TMB for all therapeutic areas and all phases of clinical development.
  • Assist in lab instrument validation.
  • Assist in the transition of biomarker assays from Basic Research to Clinical by providing technical guidance on fit-for-purpose assay validation.
  • Interface with biomarker leads and operation leads in early and late stage clinical development to execute on biomarker strategies in clinical trials.
  • Writing memos, assay validation reports, clinical sample analysis reports and publications summarizing data, and writing/updating lab SOPs.
  • Serve as a subject matter expert in immunoassay development and validation, collaborating with project teams, biomarkers leaders, clinical operation and regulatory affairs on the implementation of these assays in clinical trials.
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