Bispecifics Scientist - Fully Remote Job Syracuse New York USA,Research/Development

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 ADC and/or bispecific experts 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 across ADC and/or bispecific programs
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
Have direct experience with ADCs and/or bispecific (or multispecific) antibodies — 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 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.

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