AI Biologist – Drug Development

atLatchBioRemoteUS flagCaliforniaFull-timeArtificial IntelligenceMid-levelSenior$140k – $180k/year

Posted 2 days ago

This is a fully remote position, open to applicants in California.

πŸ“‹ Description

β€’ Participate in assessing the performance of agents throughout the drug discovery and development pipeline, from target validation to IND-enabling studies.

β€’ Convert preclinical data into decisions regarding program advancement or termination.

β€’ Develop realistic program case studies encompassing target validation, lead optimization, candidate nomination, and IND-enabling studies.

β€’ Compile multimodal preclinical data packages, including SAR/potency panels, ADME/PK profiles, in vivo efficacy, GLP toxicology, safety pharmacology, and biodistribution data.

β€’ Analyze PK/PD, GLP toxicology, and safety pharmacology results across various modalities and development phases.

β€’ Synthesize program go/no-go decisions from diverse data sources.

β€’ Review and rigorously evaluate AI agent outputs for pharmacological accuracy.

β€’ Adjust AI agent confidence levels on incomplete or contradictory preclinical data.

β€’ Collaborate with software engineers and scientists in creating datasets and AI agent tasks throughout the drug development process.


⛳️ Requirements

β€’ An advanced degree (MS/PhD/PharmD) in pharmacology, toxicology, pharmaceutical sciences, medicinal chemistry, or a related biomedical field, or equivalent experience in the industry.

β€’ Minimum of 3 years of practical experience in pharmaceutical or biotech drug discovery and development.

β€’ Direct experience with lead optimization, candidate nomination, or the design of IND-enabling studies in at least one modality.

β€’ Proficient in interpreting PK/PD, ADME, and GLP toxicology data to guide dose selection and risk evaluation.

β€’ Knowledge of IND-enabling regulatory standards and the nonclinical data package required by the FDA/EMA is advantageous.

β€’ Familiarity with GLP toxicology, safety pharmacology, genotoxicity, biodistribution, and bioanalytical assays.

β€’ Experience in assessing SAR, potency, selectivity, and developability trade-offs among candidate molecules.

β€’ Excellent scientific writing capabilities.

β€’ Competence in utilizing AI agents and the ability to discern technically accurate yet pharmacologically or practically flawed reasoning.

β€’ Comfort in navigating uncertainty and proactively identifying data or instruction gaps.

β€’ Demonstrated agency and initiative.


🏝️ Benefits

β€’ Performance-based pay linked to weekly quota achievements.

β€’ Full on-target earnings (OTE) for the duration of special projects.

β€’ Full OTE for a day if the platform experiences downtime.

β€’ Full OTE for the first four weeks during the onboarding process.

β€’ Comprehensive health, dental, and vision insurance: fully covered for you, 50% coverage for dependents.

β€’ 401(k) plan with no matching contribution.

β€’ Starting with 12 days of paid time off (PTO), increasing with promotions.

β€’ Equity opportunities.

β€’ Promotions based on performance, with OTE increases at each level.

β€’ Options for remote, hybrid, or onsite work.

β€’ Catered lunches and dinners for onsite employees.

β€’ Unlimited access to snacks.

β€’ Company outings organized most months.

β€’ Team offsite events.

β€’ H-1B sponsorship, including transfers.

β€’ O-1 sponsorship.

β€’ TN sponsorship.

β€’ Support for STEM OPT.

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