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TScan Therapeutics

Clinical Pharmacology Consultant

TScan Therapeutics

. Provide clinical pharmacology input to regulatory documents .

Posted 11/4/2026contractRemote • Massachusetts • United StatesMid-LevelSeniorWebsite

Core Competencies

Role fit
Core Competencies

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Demonstrates expertise in clinical pharmacology, including the analysis and reporting of pharmacokinetic and pharmacodynamic data. Proficient in regulatory documentation and clinical study design, with strong collaboration skills across multidisciplinary teams.

Highest-signal resume keywords
Clinical Pharmacology ExpertisePharmacokinetics AnalysisPhoenix WinNonlin ProficiencyCompartmental PK/PD ModelingRegulatory Document Preparation

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
PharmacokineticsPharmacodynamicsClinical Study DesignMathematical Model DevelopmentData AnalysisStatistical AnalysisRegulatory ComplianceTechnical DocumentationClinical Trial ProtocolsSAP Development
Soft Skills
CollaborationLeadershipCommunicationAnalytical ThinkingProblem Solving
Tools & Technologies
Phoenix WinNonlinRNONMEMMATLABClinical Operations Software
Industry Keywords
Pharmaceutical SciencesPharmacologyPharmacometricsClinical DevelopmentBiostatistics

About the role

Key responsibilities & impact
  • Provide clinical pharmacology input to regulatory documents
  • Participate in clinical study design and documentation, including lab manuals, protocols, and SAPs
  • Independently lead and oversee analysis, interpretation, integration, and reporting of clinical pharmacokinetic and pharmacodynamic data for assigned projects
  • Collaborate with Clinical Development, Biostatistics, Non-Clinical Product Development, Clinical Operations, and Regulatory
  • Monitor CRO and external vendor work for compliance with protocols, quality standards, and timelines
  • Report directly to the Head of Clinical Pharmacology

Requirements

What you’ll need
  • MS with 8+ years or Ph.D. with 3+ years in pharmaceutical sciences, pharmacology, pharmacometrics, pharmacokinetics, or related discipline, or Pharm.D. or M.D. with relevant experience
  • Publication record with demonstrated technical exposure to early exploratory trials through Phase 2/3 programs preferred
  • Experience using Phoenix WinNonlin, R, NONMEM, MATLAB, or other pharmacokinetic and modeling software
  • Compartmental PK/PD modeling experience is a plus
  • Strong mathematical model development and analytical skills

Benefits

Comp & perks
  • Contract position
  • Remote work arrangement
  • Support from 30–40 hours per week