Clinical Pharmacology Consultant

📋 Description

• Provide clinical pharmacology expertise and input for regulatory submissions and other development
• Contribute to clinical study design and the preparation and review of study documents, including
• Independently lead and oversee the analysis, interpretation, integration, and reporting of clinical
• Collaborate with cross-functional stakeholders across Clinical Development, Biostatistics
• Oversee work performed by contract research organizations (CROs) and external vendors, ensuring
• Apply scientific judgment and analytical expertise to help guide clinical development decisions and

🎯 Requirements

• Master’s degree with at least 8 years of relevant experience, Ph.D. with at least 3 years of
• Demonstrated experience in clinical pharmacology and clinical study design within the biotechnology
• Strong understanding of clinical PK/PD data analysis, interpretation, integration, and reporting.
• Experience with pharmacokinetic analysis and modeling software, such as Phoenix WinNonlin, R
• Strong mathematical modeling, quantitative analysis, problem-solving, and scientific communication
• Experience spanning early exploratory clinical trials through Phase 2 or Phase 3 programs is

🎁 Benefits

• Remote flexibility: Work remotely from within the United States.
• Contract engagement: A flexible consulting opportunity offering approximately 30–40 hours per week.
• Scientific impact: Contribute to clinical-stage development programs targeting rare and inherited
• Cross-functional collaboration: Partner with experts across clinical development, biostatistics
• Professional contribution: Apply advanced clinical pharmacology and quantitative modeling expertise
• Compensation and additional benefits: Salary or hourly rate, healthcare coverage, paid time off