PK Scientist

This is a fully remote position, open to applicants in United Kingdom.

📋 Description

• Develop and oversee the creation of clinical pharmacology trial protocols, ensuring timely review, approval, and distribution.

• Conduct preliminary, interim, and final pharmacokinetic (PK), pharmacodynamic (PD), and PK/PD analyses utilizing non-compartmental methods.

• Formulate the Clinical Pharmacology Analysis Plan (CPAP) and prepare data handling logbooks before the final Non-Compartmental Analysis (NCA).

• Generate tables, listings, and figures, and assist in composing clinical pharmacology sections of Clinical Study Reports (CSRs).

• Perform quality control reviews of protocols, analyses, datasets, and all deliverables, ensuring adherence to standard operating procedures (SOPs), ICH-GCP, and regulatory standards.

⛳️ Requirements

• A Bachelor’s degree or higher in a scientific field (or equivalent experience) with proficient written and verbal communication abilities.

• Over 4 years of relevant experience in clinical pharmacology, including familiarity with clinical study protocols and regulatory standards.

• Strong practical knowledge of PK & PD software applications.

• Practical experience with Phoenix WinNonlin and a working understanding of R for PK/PD analysis (Experience with R is a plus).

• Superior data-handling capabilities and familiarity with database architectures.

• Proficient understanding of noncompartmental PK analysis & PK/PD evaluations.

🏝️ Benefits

• Competitive base salary along with performance-based incentives.

• Health and wellness programs, including medical, dental, and vision coverage as applicable.

• Retirement and pension options.

• Life insurance and disability coverage.

• Employee assistance programs and wellness resources.

• Opportunities for learning and development through structured training and career pathways.