Pharmacokineticist

About the Job Join Excelya, where Audacity, Care, and Energy define who we are and how we work. We are committed to creating innovative solutions and fostering a collaborative and inclusive work environment. The consultant will contribute to pharmacokinetics (PK) activities across Phase I to Phase III clinical trials, ensuring the timely delivery of high‑quality PK analyses, interpretations, and documentation. This role involves close collaboration with clinical, non-clinical, and modeling teams to deliver robust pharmacokinetic data and modeling outputs that inform drug dosing strategies and regulatory submissions.

Main responsibilities: • Contribute to the definition and implementation of PK strategies across clinical studies. • Write and review pharmacokinetic sections of clinical study protocols. • Support study set‑up, conduct, and follow‑up from a PK perspective. • Perform pharmacokinetic analyses, primarily using Non‑Compartmental Analysis (NCA). • Interpret preliminary and final PK data and translate results into clear conclusions. • Present PK results during internal project team meetings. • Contribute to Clinical Study Reports (CSR) and/or standalone PK reports. • Collaborate with cross‑functional teams including Clinical Operations, Biostatistics, and Data Management. • Ensure all PK activities are delivered in line with study timelines and quality standards.