About this role
Shape clinically plausible pharmacology datasets and supporting scientific content for multiple workflows, with responsibility for ensuring pharmacokinetic and pharmacodynamic outputs align with efficacy and safety results.
Key Responsibilities- Simulate the clinical pharmacology layer of each data room, including PK and PD datasets, dosing and escalation regimens, exposure-response relationships, and bioanalytical reports.
- Ensure dose rationale and concentration data are clinically plausible and reconcile with efficacy and safety outputs.
- Author dose-selection rationale, drug concentration and response sections, and content addressing drug-drug and drug-disease interactions.
- Design prompts, reference outputs, and evaluation rubrics to measure an AI agent''s ability to complete comparable clinical pharmacology work.
- PharmD, MD, PhD in pharmacology, pharmacokinetics, or a related field, or equivalent.
- At least 5 years of experience required; 10 to 25 years preferred.
- Experience supporting pre-market Phase 1, 2, or 3 programs as a clinical pharmacologist.
- Hands-on expertise in PK/PD, dose selection and escalation, and exposure-response analysis.
- First-in-human program experience is strongly preferred.
- Ability to work from a protocol and statistical analysis plan to produce pharmacology data that withstands expert review.
- Remote, hourly engagement.
- Minimum availability of 20 to 25 hours per week; 30 or more hours per week preferred.
$120 to $170 per hour.
EligibilityApplicants must be located in the United States, Canada, or France.