Director of Pharmacometrics

Konsus, Inc. (Superside); United States; Remote; USD 130,000 - 170,000; Full time

Job summary

A leading company is seeking a Senior Associate Director/Director of Pharmacometrics for a remote position. The role involves developing PMx strategies, overseeing clinical developments, and leveraging expertise in pharmacology and regulatory guidelines. Ideal candidates have strong educational backgrounds and extensive experience in clinical settings.

Qualifications

• At least six years of relevant experience with a Master's or four years with a PhD.
• Minimum of five years of relevant experience with a professional degree in pharmacy or medicine.
• Two to four years of experience in clinical development teams preferred.

Responsibilities

• Develop PMx strategy and contribute to clinical development plans.
• Deliver high-quality PMx analyses for decision-making during clinical drug development.
• Manage projects with external organizations.

Skills

Proficiency in PMx software

Broad knowledge in clinical pharmacology

Education

Master's Degree in Medicine, Pharmacometrics, Clinical Pharmacology, Pharmacy, Mathematics, Biology, Statistics

PhD in relevant field

Job description

A company is looking for a Senior Associate Director/Director of Pharmacometrics (Remote).

Key Responsibilities

• Develop PMx strategy and contribute to clinical development plans, implementing model-informed drug discovery and development
• Deliver high-quality PMx analyses and internal documents for decision making throughout clinical drug development
• Represent Clinical Pharmacology/PMx in project teams and manage projects with external organizations

Required Qualifications and Education

• Master's Degree in Medicine, Pharmacometrics, Clinical Pharmacology, Pharmacy, Mathematics, Biology, Statistics, or equivalent with at least six years of relevant experience; or a PhD with four years of experience
• Professional degree in pharmacy or medicine with a minimum of five years of relevant experience
• Proficiency in PMx software (e.g., NONMEM, Monolix, R, SAS, PBPK software)
• Two to four years of experience in clinical development teams preferred
• Broad knowledge in clinical pharmacology, clinical drug development, and regulatory guidelines