Senior PK Scientist at ICON is a pivotal role within our global healthcare intelligence and clinical research organization, dedicated to accelerating the delivery of new medicines to patients. We are looking for an experienced Clinical Pharmacology professional to contribute to protocol development and PK/PD analysis across Phase I–IV clinical trials.

The Role

You will be responsible for authoring and coordinating the development of clinical pharmacology trial protocols, ensuring timely review, approval, and issuance. Your day-to-day activities will include performing preliminary, interim, and final PK, PD, and PK/PD analyses using non-compartmental methods, developing the Clinical Pharmacology Analysis Plan (CPAP), and generating data handling logbooks prior to final NCA. Additionally, you will create tables, listings, and figures, and contribute to drafting clinical pharmacology sections of Clinical Study Reports (CSRs). Conducting QC reviews of protocols, analyses, datasets, and all deliverables while ensuring compliance with SOPs, ICH-GCP, and regulatory requirements will also be part of your responsibilities.

Requirements

• Bachelor’s degree or higher in a scientific discipline (or equivalent experience).
• 4+ years of relevant experience in clinical pharmacology, including exposure to clinical study protocols and regulatory requirements.
• Excellent hands-on knowledge of PK & PD software packages.
• Hands-on experience with Phoenix WinNonlin and working knowledge of R for PK/PD analysis (Experience with R is an advantage).
• Excellent data-handling skills and working knowledge of database structures.
• Working knowledge of non-compartmental PK analysis & PK/PD analyses.

What We Offer

• Competitive base salary and performance-related incentives.
• Health and wellbeing programmes including medical, dental, and vision coverage where applicable.
• Retirement and pension plans.
• Life assurance and disability coverage.
• Employee assistance programmes and wellbeing resources.
• Learning and development opportunities through structured training and career pathways. Benefits may vary depending on role and location. Visit our careers site to read more about the benefits ICON offers.

If you require reasonable accommodations during the recruitment process, please let us know or submit a request here. Join us at ICON, where you can make a meaningful difference in patients' lives as part of a world-class clinical research organization. If you’re as driven as we are, we invite you to connect with us.