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Preclinical R&D Scientist, ADC & Bispecifics, for AI Model Training

Cedar Park, TX

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Job description

Apply hands-on preclinical drug-development expertise to help improve AI models for chemistry, materials science, and drug discovery. This remote opportunity combines wet-lab and translational R&D experience with scientific data review, annotation, and expert input across antibody-drug conjugate and bispecific programs.

Key Responsibilities Review technical materials and real-world R&D data from ADC and/or bispecific programs.

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

Advise on scientific and development decisions, including target and modality selection, optimization, trade-offs, and risk.

Help establish structure and quality standards for a scientific dataset pipeline.

Participate in expert discussions, interviews, and research engagements.

Work directly with the client team.

Qualifications Hands-on, non-administrative preclinical R&D experience at a company that develops drug assets in-house and has advanced programs to the clinic.

Direct experience with ADCs and/or bispecific or multispecific antibodies.

Experience in a core R&D function, such as discovery biology, medicinal chemistry, protein or antibody engineering, computational science, in vivo or translational research, pharmacology or PK-PD, toxicology, or CMC or formulation.

5+ years of relevant industry R&D experience, with flexibility based on depth of experience.

Experience advancing a program through lead optimization or IND-enabling and preclinical development is preferred.

Experience at a mid-sized, emerging, or resource-constrained biotech is preferred, ideally with current experience outside a top-20 pharmaceutical company.

Role Fit This role is intended for hands-on preclinical R&D professionals, from individual contributor through Director level. It is generally not suited to candidates whose work is primarily CRO or CDMO services, academic-only research, QC or analytical work, clinical development only, diagnostics, or regulatory or medical writing.

Work Terms Remote, hourly engagement.

Part-time schedule of roughly 10 hours per week.

Compensation $60 to $100 per hour.

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