Preclinical R&D Expert, In-house Drug Development

Mercor
Sciences and research
Remote
Contract

$60 to $100/hIndicative range provided by Mercor

Posted on August 15, 2026 · Applications until December 2, 2026

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This remote role involves reviewing technical materials, annotating scientific data, and providing expert perspective to improve AI models for drug discovery. Candidates must have at least five years of hands-on preclinical research and development experience in a core function with specific drug modalities.

Description in English, as published by Mercor.

Mercor is partnering with a venture-backed AI lab building frontier AI platforms and physics-based foundation models for chemistry, materials science, and drug discovery. They're extending their platform into new areas of pharmaceutical development and are looking for hands-on preclinical R&D experts across drug modalities to help guide what they build.

Are you a preclinical R&D scientist who has taken drug programs from the bench toward the clinic, and curious how AI is reshaping drug discovery? This is a hands-on role that blends your wet-lab and translational experience with a growing understanding of how scientific data trains the next generation of AI models.

In this role, you'll:

  • Review technical materials and real-world R&D data in your area of expertise

  • Label, classify, and annotate scientific data and model outputs to improve model performance

  • Provide expert perspective on key scientific and development decisions (target/modality selection, optimization, trade-offs, risk)

  • Help define structure and quality standards for the client's dataset pipeline

  • Participate in expert discussions, interviews, and research engagements

You're a strong fit if you:

  • Have hands-on, non-administrative preclinical R&D experience at a company that develops its own drug assets in-house and has taken programs to the clinic, Must Have

  • 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, Must Have

  • Have hands-on experience with one or more drug modalities (small molecules, monoclonal antibodies, peptides, ADCs, bispecifics, mRNA, siRNA, ASOs, PROTACs, molecular glues, cell therapies, gene therapies, radioligand therapies, etc.), Must Have

  • Have 5+ years of relevant industry R&D experience (flexible based on depth)

  • Have taken a program through lead optimization or IND-enabling/preclinical development (nice to have)

  • Have experience at mid-sized, emerging, or resource-constrained biotech, ideally currently outside the top-20 pharmaceutical companies (nice to have)

This is a hands-on preclinical R&D role, likely not the right fit if your work is mainly CRO/CDMO services, academic-only, QC/analytical-only, clinical-development-only, diagnostics, or regulatory/medical-writing.

Your work will directly feed into the models reshaping how medicines are discovered, helping intelligent systems reason about real-world pharmaceutical R&D.

Here are more details about the role:

  • You will interface directly with the client team.

  • This is an ongoing, part-time engagement of roughly 10 hours per week.

  • Seniority welcome from individual contributor through Director.

10 openings

Open worldwide

About Mercor

Mercor is a US marketplace hiring remote experts for AI and consulting projects, from law to engineering. The original posting is on their site.

View this job on Mercor

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