Principal Scientist/Director, Translational Pharmacology

5AM Ventures

$180K — $230K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • PhD, MD, or equivalent in pharmacology, biomedical sciences, or related field
  • Significant preclinical pharmacology experience in biotech or pharmaceutical environments
  • Experienced in selecting relevant animal models for research
  • In-depth knowledge of PK/PD modeling and chemical kinetics
  • Proficient in designing studies for drug combinations using factorial design
  • Hands-on experience with IND-enabling studies and contributions to IND submissions
  • Strong statistical and data analysis capabilities
  • Familiarity with metabolic diseases like obesity and diabetes is a plus.

Responsibilities

  • Lead and execute preclinical pharmacology studies for drug development
  • Develop quantitative PK/PD models to optimize dosing strategies
  • Design and oversee in vivo studies with appropriate animal models
  • Perform rigorous data analysis to drive decision-making
  • Translate preclinical results into clinically relevant strategies
  • Collaborate with teams to refine drug candidates and delivery systems
  • Contribute to regulatory documentation and IND study requirements
  • Build and maintain relationships with CROs and collaborators.

Benefits

  • Comprehensive health benefits
  • Performance bonuses
  • Equity participation
Full Job Description
We are seeking a highly motivated, hands-on Director of Translational Pharmacology to lead and drive preclinical pharmacology efforts across our pipeline. This individual will play a central, decision-making role in translating innovative science into rigorous, in vivo proof-of-concept and clinically actionable pharmacology strategies.

  • Lead the design, execution, and interpretation of preclinical pharmacology studies supporting drug discovery and development programs
  • Develop and apply quantitative PK/PD models, integrating pharmacokinetics, pharmacodynamics, and chemical kinetics to guide compound optimization and dosing strategies
  • Design and oversee in vivo studies, including selection and development of appropriate animal models
  • Drive rigorous data analysis, including statistical evaluation and modeling to inform decision-making
  • Translate preclinical findings into clinically relevant hypotheses and development strategies
  • Collaborate closely with teams to optimize drug candidates and delivery systems
  • Contribute to regulatory documentation and strategy (IND-enabling studies, study reports, etc.)
  • Build and manage relationships with CROs and external collaborators


Qualifications

  • PhD, MD, or equivalent in pharmacology, biomedical sciences, or related field
  • Significant experience in preclinical pharmacology within biotech or pharmaceutical settings
  • Experience in choosing appropriate animal models
  • Deep expertise in PK/PD modeling, with strong grounding in chemical kinetics and quantitative biology
  • Proven experience designing studies to evaluate drug combinations and synergy, including application of factorial experimental design Demonstrated experience designing and interpreting in vivo pharmacology studies
  • Experience in advancing preclinical candidates through IND-enabling studies and contributing meaningfully to IND submissions
  • Strong statistical and data analysis skills
  • Experience in metabolic diseases, particularly obesity and/or diabetes, strongly preferred


$180,000 - $230,000 a year

Final compensation will be based on a candidate's qualifications, experience, and geographic location. Employees are also eligible for performance bonuses, equity participation and comprehensive health benefits.

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