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Hybrid | Senior Pharmaceutical R&D Scientist

Job in San Francisco, San Francisco County, California, 94102, USA
Listing for: 24-MAG LLC
Full Time, Part Time position
Listed on 2026-08-24
Job specializations:
  • Research/Development
    Pharmaceutical Science/ Research, Research Scientist
  • Pharmaceutical
    Pharmaceutical Science/ Research
Salary/Wage Range or Industry Benchmark: 65 - 105 USD Hourly USD 65.00 105.00 HOUR
Job Description & How to Apply Below
Position: Hybrid | Senior Pharmaceutical R&D Scientist — $65–$105/hour

Senior Pharmaceutical And Biotechnology R&D Professional Opportunity

We are sharing a specialised full-time opportunity for senior pharmaceutical and biotechnology R&D professionals with substantial experience across drug discovery, preclinical development, translational science, clinical development, regulatory affairs, or CMC.

This role supports advanced research focused on improving how AI systems reason through real-world pharmaceutical research and development work. Selected professionals will review complex scientific tasks and outputs, develop authoritative reference solutions and instructions, and translate practical drug-development judgement into rigorous standards for high-quality scientific reasoning.

Key Responsibilities
  • Evaluate pharmaceutical research and development tasks for scientific accuracy, completeness, and professional realism
  • Review outputs for unsupported efficacy or safety claims, weak reasoning, missing considerations, and flawed assumptions
  • Identify conclusions that appear plausible but would not withstand scientific or regulatory scrutiny
  • Assess whether recommendations and interpretations are appropriately supported by available evidence
  • Apply senior-level judgement across complex drug-development scenarios
  • Develop and review tasks involving target identification, validation, and early discovery strategy
  • Evaluate biological rationale, experimental evidence, and translational relevance
  • Assess whether proposed discovery approaches are scientifically credible
  • Identify gaps in target validation or mechanistic reasoning
  • Create reference solutions reflecting realistic pharmaceutical R&D workflows
  • Review problems involving compound optimisation, SAR, potency, selectivity, and develop ability
  • Evaluate trade-offs across efficacy, safety, pharmacokinetics, and physicochemical properties
  • Assess medicinal chemistry strategies and compound progression decisions
  • Identify unsupported assumptions in lead-selection reasoning
  • Apply practical understanding of discovery-stage decision-making
  • Develop and evaluate scenarios involving pharmacology, toxicology, PK/PD, and preclinical development
  • Review study design, interpretation, and evidence quality
  • Assess safety findings and translational implications
  • Determine whether conclusions are proportionate to available data
  • Identify missing studies, weak controls, or incomplete development logic
  • Review tasks involving translational strategy and biomarker development
  • Evaluate links between preclinical findings and clinical hypotheses
  • Assess biomarker selection, validation, and interpretation
  • Identify gaps between mechanistic evidence and proposed clinical application
  • Develop reference outputs representing strong translational reasoning
  • Contribute expertise across clinical development, regulatory strategy, and CMC where relevant
  • Evaluate development plans, evidence packages, and programme decisions
  • Review questions involving clinical progression, regulatory requirements, and manufacturing considerations
  • Assess whether development recommendations align with scientific and operational constraints
  • Identify unsupported conclusions or missing requirements within complex development scenarios
  • Write detailed task instructions reflecting authentic pharmaceutical R&D workflows
  • Produce high-quality reference solutions to complex drug-discovery and development problems
  • Define what constitutes a complete, scientifically credible, and professionally defensible response
  • Translate tacit development judgement into explicit evaluation criteria
  • Develop new tasks based on realistic industry decision-making
  • Collaborate with research teams and specialists from adjacent scientific disciplines
  • Help maintain consistent standards across pharmaceutical-related evaluation work
  • Identify recurring weaknesses and failure patterns in model outputs
  • Refine evaluation criteria based on review findings
  • Contribute domain expertise to new pharmaceutical research workflows
Ideal Profile
  • PhD or PharmD in a pharmaceutically relevant discipline such as Medicinal Chemistry, Organic Chemistry, Pharmacology, Molecular Biology, Pharmaceutical Sciences, Toxicology, or a related field
  • MD candidates may also qualify where they…
Position Requirements
10+ Years work experience
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