Principal Pharmacokinetics Scientist

🔥 16 hours ago

🇺🇸 United States – Remote

⏰ Full Time

🔴 Lead

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ClinChoice

WebsiteLinkedInAll Job Openings

1001 - 5000 employees

Founded 1998

💼 Consulting

🏥 Healthcare

📦 Logistics

Consulting • Healthcare • Logistics

ClinChoice is a global full-service contract research organization (CRO) established in 1995, specializing in clinical development, post-marketing, and functional service support for the pharmaceutical, biotechnology, and medical devices industries. They provide comprehensive solutions from early clinical development to post-approval lifecycle management, with expertise in a variety of therapeutic areas such as autoimmune and inflammation, dermatology, endocrinology, infectious diseases, neuroscience, and oncology. ClinChoice aims to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices. The company supports its clients with clinical, regulatory, and operational expertise across all phases of product development.

📋 Description

• Lead study concept and protocol design • Author clinical pharmacology development plans and create modeling and simulation plans • Conduct PK-PD, Pop PK-PD, and related analyses supporting clinical trials • Interpret and integrate data into regulatory filings, clinical publications, and presentations • Provide technical expertise using PK/PD data analysis software • Collaborate with clients and cross-functional teams to deliver project outcomes • Prepare and review PK/PD analysis reports • Apply pharmaceutical regulatory requirements to support compliant submissions • Mentor junior pharmacologists and implement team best practices • Stay current with clinical pharmacology advancements

🎯 Requirements

• PhD in pharmaceutical sciences, pharmacology, life sciences, clinical pharmacology, pharmacokinetics, or a related discipline, with at least 3 years of relevant research or clinical experience in clinical pharmacology and pharmacokinetic-pharmacodynamic modeling within the pharmaceutical or biotechnology industry • PharmD in a relevant discipline with a minimum of 5 years of experience in clinical pharmacology and PK/PD modeling and simulation • Alternatively, a Master’s degree in a related field with at least 7 years of relevant experience in Clinical Pharmacology and Modeling & Simulation • Robust knowledge of pharmacokinetics, pharmacodynamics, translational sciences, and PK/PD data analysis • Hands-on experience and expertise with Phoenix WinNonlin, NLME, R/R Studio, Monolix, and NONMEM • Strong communication and organizational skills, with the ability to present complex data to scientific and non-scientific audiences • Proven ability to manage multiple projects simultaneously in a dynamic, client-oriented environment • Preferred: experience across a variety of therapeutic areas • Preferred: prior CRO experience • Relevant certifications are a plus

🏖️ Benefits

• Professional development and continuous training • Work-life balance • Collaborative “one-team” culture • Equal opportunity and diversity-focused workplace