Clinical Pharmacologist – PK/PD, Dose Strategy

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🌐 United States, Canada, +1 more countries – Remote

🇺🇸 United States – Remote 🇨🇦 Canada – Remote 🇫🇷 France – Remote

🗽 New York – Remote

🗽 New York – Remote

💵 $110 - $160 / hour

⏱ Part Time

🟡 Mid-level

🟠 Senior

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24-MAG

WebsiteLinkedInAll Job Openings

2 - 10 employees

🤝 B2B

💼 Consulting

B2B • Consulting

24-MAG is a commercial strategy and execution firm that helps B2B organizations design and implement systems, workflows, and operating rhythms for sales, client management, and cross-functional projects. They focus on transforming scattered processes into aligned, measurable, and scalable commercial functions—covering pipeline structure, account management frameworks, and operational discipline for teams seeking efficient, intentional growth.

📋 Description

• Develop and validate synthetic clinical pharmacology datasets • Create realistic PK and PD data aligned with study protocols and development objectives • Reconcile dosing, concentration, efficacy, and safety information across the broader clinical data package • Review pharmacology outputs for clinical plausibility and internal consistency • Evaluate concentration-time profiles, exposure metrics, and pharmacodynamic responses • Assess dose, exposure, response, and safety relationships • Develop and review dose-selection rationales and dose-escalation strategies • Assess starting-dose, escalation, expansion, and recommended-dose decisions • Integrate PK, PD, efficacy, and safety information into dose rationales • Develop and assess exposure-response relationships across efficacy and safety endpoints • Review assumptions, covariates, and concentration-response findings • Translate quantitative findings into clinical-development recommendations • Develop and review drug-drug and drug-disease interaction content • Review bioanalytical reports and concentration datasets • Design clinical pharmacology assignments based on Phase I–III workflows • Produce authoritative reference outputs and define evaluation criteria for complex pharmacology scenarios

🎯 Requirements

• 5+ years of professional clinical pharmacology experience; 10–25 years preferred • Demonstrated experience supporting pre-market Phase I–III clinical programmes • Strong hands-on expertise in PK/PD analysis • Direct experience with dose selection and dose-escalation strategy • Strong experience with exposure-response analysis • Comfortable working from clinical protocols and Statistical Analysis Plans • Experience developing pharmacology outputs that integrate with efficacy and safety datasets • First-in-human clinical development experience strongly preferred • PharmD, PhD in Pharmacology, Pharmacokinetics, or a related field, MD, or equivalent advanced qualification • Strong quantitative and clinical judgement • Excellent written communication and ability to explain complex pharmacology conclusions precisely • Based in the United States, Canada, or France • Minimum availability of approximately 20–25 hours per week • Work must be completed without using confidential or proprietary information belonging to any employer, sponsor, client, institution, or other third party • H1-B and STEM OPT support is unavailable for this engagement

🏖️ Benefits

• Part-time independent contractor engagement • Fully remote • Flexible scheduling based on project requirements • Projects may be extended, shortened, or concluded based on project needs and performance