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.
Requirements
Experience: Proven experience in pharmacokinetic analysis and modeling, preferably within pharmaceutical research and development.
Skills:
- Strong expertise in Non‑Compartmental Analysis (NCA).
- Knowledge of PK/PD modeling is an advantage.
- Practical experience with Phoenix WinNonlin or equivalent PK software.
- Familiarity with R and data visualization tools is a plus.
Education: Advanced degree (Master’s or Ph.D.) in Pharmacokinetics, Pharmacology, or Pharmaceutics
Languages: Fluency in French and English.
Benefits
Why Join Us?
At Excelya, we combine passion for science with enthusiasm for teamwork to redefine excellence in healthcare.
Here's what makes us unique—
We are a young, ambitious health company representing 900 Excelyates, driven to become Europe's leading mid-size CRO with the best employee experience. Our one-stop provider service model — offering full-service, functional service provider, and consulting — enables you to evolve through diverse projects. Working alongside preeminent experts, you will help improve scientific, operational, and human knowledge to enhance the patient's journey.
Excelling with care means benefiting from an environment that values your natural talents, pushes boundaries with audacity, and nurtures your potential, allowing you to contribute fully to our shared mission.
Skills Required
- Proven experience in pharmacokinetic analysis and modeling
- Strong expertise in Non-Compartmental Analysis (NCA)
- Practical experience with Phoenix WinNonlin or equivalent PK software
- Advanced degree in Pharmacokinetics, Pharmacology, or Pharmaceutics
- Fluency in French and English
What We Do
Excelya is an independent partner that serves Biotech, Pharma, and Medical Device organizations with a comprehensive range of Full-service CRO, FSP, and Resourcing solutions guided by compassion, care, and excellence. Founded in 2014 and headquartered in Paris, France, and operating in 28 countries across Europe, USA and India, Excelya has a global team of 900+ experts who understand the critical needs of clients to provide bespoke and robust trial solutions across a broad spectrum of therapeutic areas, with speciality focus on Oncology & Hematology, Rare Disease & Pediatrics, Infectious Disease, Inflammation & Immunotherapy, Pain Treatment & CNS, and Late Phase & RWE.
