PK Scientist

At ICON, we're committed to fostering an inclusive environment that drives innovation and excellence in clinical development. As a PK Scientist, you'll play a crucial role in shaping the future of clinical development.

• Author and coordinate the development of clinical protocols, ensuring timely approval and issuance.
• Provide quality control review of protocols as needed.
• Review dataset requirements for clinical studies with non-compartmental analysis.
• Write the Clinical Pharmacology Analysis Plan (CPAP) based on the protocol.
• Generate a logbook with data handling rules prior to the final NCA.
• Perform preliminary, interim, and final PK, PD, and/or PK/PD analysis for trials in all phases of drug development.
• Create tables, listings, and figures based on the CPAP.
• Draft the clinical pharmacology sections of the Clinical Study Report.
• QC analysis, all delivered outputs, and documents reporting the analysis.

• Minimum degree: BA/BS in a health, science, or computer science related field.
• 3 years' industry experience.
• Working knowledge of Phoenix WinNonlin is essential.
• Working knowledge of Microsoft suite of software.
• Knowledge of noncomparmental PK analysis and statistical principles.
• Demonstrated written and verbal communication.

We offer a comprehensive and competitive total reward package, including an excellent level of base pay, variable pay, and recognition programs. Our best-in-class employee benefits, supportive policies, and wellbeing initiatives are tailored to support you and your family at all stages of your career.

We're committed to developing our employees in a continuous learning culture, where every experience adds to your professional development. ICON is an equal opportunity and inclusive employer, committed to providing a workplace free of discrimination and harassment.