Preclinical R&D Expert – In-house Drug Development (Train AI Models Part Time!)

## About the Role 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? Our client is a venture-backed AI lab building frontier AI platforms and physics-based foundation models for chemistry, materials science, and drug discovery. They want hands-on experts across drug modalities to help guide what they build. ## 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.) - 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. ## Role details: - You'll interface directly with the client team - Remote · hourly · seniority welcome from individual contributor through Director