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Advisor - Antibody Developability Validation & Benchmarking

Job in Boston, Suffolk County, Massachusetts, 02298, USA
Listing for: Initial Therapeutics, Inc.
Full Time position
Listed on 2026-06-18
Job specializations:
  • Research/Development
    Research Scientist
Salary/Wage Range or Industry Benchmark: 200000 - 250000 USD Yearly USD 200000.00 250000.00 YEAR
Job Description & How to Apply Below

Lilly is a global healthcare leader headquartered in Indianapolis, Indiana. We discover and bring life‑changing medicines to help people around the world.

Organization Overview

We make a difference for people around the world by discovering, developing, and delivering medicines that help individuals live longer, healthier, and more active lives. We also support communities through philanthropy and volunteerism.

Purpose

Lilly Tune Lab is an AI‑powered drug discovery platform that provides biotech companies with access to machine learning models trained on Lilly’s proprietary pharmaceutical research data. Through federated learning, the platform enables Lilly to build models on broad, diverse datasets from across the biotech ecosystem while preserving partner data privacy and competitive advantages. Antibody develop ability prediction is a core workstream within Tune Lab—covering aggregation, self‑association, polyspecificity, thermal stability, viscosity, and chemical liabilities—that gates progression from discovery into lead optimization, cell line development, and formulation.

The Advisor/Senior Advisor – Antibody Develop ability Validation & Benchmarking plays an essential role in establishing whether Tune Lab’s federated antibody models can be trusted to triage real candidates. This validation‑led role requires deep understanding of antibody characterization, develop ability determinants, and how predictions from a federated model translate into go/no‑go decisions in the discovery pipeline.

The role contributes to model design choices. The person will partner closely with antibody modeling scientists on architecture, feature design, and uncertainty quantification—not just downstream of them.

Key Responsibilities

Build the canonical benchmark suite covering the full develop ability portfolio—aggregation propensity (AC‑SINS, SMAC, CIC), thermal stability (nanoDSF/DSF), polyspecificity (BVP‑ELISA, Heparin RT, PSR), self‑interaction, viscosity, chemical liabilities (deamidation, isomerization, oxidation, N‑glycosylation in CDRs), and immunogenicity surrogates. Define which endpoints are evaluated jointly versus independently and how multi‑endpoint reliability rolls up to a triage decision.

Architect privacy‑preserving protocols for constructing representative test sets across distributed partner datasets, with splitting strategies appropriate to antibody data—germline‑based, CDR‑similarity‑based, and clonotype‑based splits that genuinely test generalization rather than near‑duplicate memorization.

Systematically benchmark federated antibody models against established external resources—SAbDab, OAS, TAP, the Jain et al. clinical‑stage antibody panel, FLAb, and equivalent emerging datasets—to characterize generalization gaps and quantify where federated training delivers measurable lift over public‑only baselines.

Develop validation strategies that assess model generalization across modalities and formats relevant to antibody develop ability—IgG vs. bispecific vs. fragment formats, different expression systems, different assay protocols across partners—while respecting partner data boundaries.

Implement temporal‑split and sequence‑similarity‑aware validation protocols that simulate prospective deployment, detect concept drift as partner data accumulates, and surface systematic failure modes across CDR length distributions, germline families, and physicochemical regimes.

Work alongside antibody modeling scientists on architectural and feature choices that have direct validation implications—uncertainty quantification approaches, calibration strategies, structure‑aware vs. sequence‑only representations, and how predictions from different endpoints should be combined or kept independent.

Design statistically powered validation studies that account for multiple testing across endpoints, hierarchical structure in antibody data, and non‑independent observations. Provide honest confidence intervals on reported model performance.

Build robust MLOps pipelines ensuring complete reproducibility of federated experiments, including versioning of data snapshots, model checkpoints, and hyperparameter configurations.

Develop…

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