Remote Preclinical R&D Expert – Drug Development

mercor

France

Remote

EUR 105,000 - 175,000

Full time

14 days+
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Job summary

Mercor is seeking a Preclinical R&D Expert – In-house Drug Development for a contract role. This remote position focuses on applying hands-on preclinical R&D expertise to support AI-driven drug discovery and development.

You will review technical materials and real-world data, label and annotate outputs, contribute to target and modality decisions, and help set data quality standards for the client’s dataset pipeline, leveraging 5+ years in industry R&D.

Qualifications

  • Hands-on, non-administrative preclinical R&D experience at a company that develops its own drug assets.
  • Work in a core R&D function: discovery biology, medicinal chemistry, protein/antibody engineering, computational, in vivo/translational, pharmacology/PK-PD, toxicology, or CMC/formulation.
  • Hands-on experience with one or more drug modalities (small molecules, monoclonal antibodies, peptides, ADCs, bispecifics, mRNA, siRNA, ASOs, PROTACs, etc.).
  • 5+ years of relevant industry R&D experience.

Responsibilities

  • Review technical materials and real-world R&D data in your area of expertise to improve AI model performance.
  • Label, classify, and annotate scientific data and model outputs to enhance model accuracy.
  • Provide expert perspective on key scientific and development decisions, including target and modality selection.
  • Help define structure and quality standards for the client's dataset pipeline.
  • Participate in expert discussions, interviews, and research engagements to guide AI platform development.

Skills

R&D experience
Preclinical work
Drug modalities

Job description

Mercor is seeking a Preclinical R&D Expert – In-house Drug Development for a contract role. This remote position focuses on applying hands-on preclinical R&D expertise to support AI-driven drug discovery and development.

You will review technical materials and real-world data, label and annotate outputs, contribute to target and modality decisions, and help set data quality standards for the client’s dataset pipeline, leveraging 5+ years in industry R&D.

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