Pharmacology Specialist Remote Role
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Job Location:
Monthly Salary:
Posted on:
16 hours ago
Vacancies:
1 Vacancy
Job Summary
About the job
Mercor connects elite creative and technical talent with leading AI research labs. Headquartered in San Francisco our investors include Benchmark General Catalyst Peter Thiel Adam DAngelo Larry Summers and Jack Dorsey.
Position: Drug Discovery Scientist / Toxicology Expert
Type: Contract
Compensation: $70$100/hour
Location: Remote
Role Responsibilities
- Review and annotate datasets related to drug discovery pharmacology and safety biology. Interpret experimental outputs from target biology studies biochemical assays cellular models and safety screens.
- Analyze relationships between compound structure potency selectivity exposure and toxicity signals. Identify mechanistic explanations behind efficacy or toxicity findings across discovery experiments.
- Audit annotated scientific datasets for biological pharmacological and safety accuracy. Validate structureactivity relationships (SAR) target engagement logic and pharmacokinetic interpretations.
- Contribute to annotation guidelines for drug discovery workflows SAR pharmacokinetics and ADME reasoning toxicity mechanisms and safety pharmacology.
- Review AI-generated reasoning traces involving drug mechanism of action target biology interpretation toxicity mechanisms and risk assessment. Provide structured feedback to improve scientific rigor causal reasoning and translational relevance in model outputs.
- Contribute to scientific standards documentation and training materials for model development. Help define gold-standard examples of drug discovery reasoning and toxicity interpretation.
Qualifications
Must-Have
- PhD PharmD DVM MD or MS with significant industry experience in Medicinal Chemistry Pharmacology Toxicology Chemical Biology Molecular Biology Pharmaceutical Sciences or Biochemistry.
- 35 years of hands-on experience in drug discovery or safety assessment including drug discovery programs from target validation through lead optimization SAR analysis pharmacokinetics (PK) and ADME interpretation and toxicology and safety pharmacology studies.
- Strong expertise in target biology and mechanism-of-action reasoning dose-response relationships and exposure margins and translational interpretation between preclinical and clinical findings.
- Experience reviewing primary experimental data and study reports.
- Exceptional attention to scientific accuracy and mechanistic reasoning.
Preferred
- Experience in pharmaceutical or biotechnology drug discovery teams.
- Background in lead optimization translational biology or nonclinical safety.
- Familiarity with DMPK workflows safety biomarkers and regulatory toxicology considerations.
- Experience contributing to cross-functional discovery teams.
- Exposure to AI/ML tools applied to biomedical research.
Application Process (Takes 2030 mins to complete)
- Upload resume
- AI interview based on your resume
- Submit form
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PS: Our team reviews applications daily. Please complete your AI interview and application steps to be considered for this opportunity.
