Loading ...
Loading ...
Quantitative Clinical Pharmacology Lead
Aussicht: 125
Update Tag: 26-11-2025
Ort: Braine-l’Alleud Walloon Brabant
Kategorie: Gesundheit / Medizinische Versorgung
Industrie: Pharmaceutical Manufacturing
Position: Mid-Senior level
Jobtyp: Full-time
Loading ...
Jobinhalt
Make your mark for patientsAt UCB everything we do starts with a simple question: “How will this make a difference to the lives of people living with severe diseases?” We do that by connecting our ground-breaking science with patients and their families around the world living with the physical and social burdens of autoimmune and neurological disorders. Those connections offer new perspectives, drive innovation, and offer the hope of a new generation of therapies that will help improve lives on a global scale.To strengthen the Quantitative Clinical Pharmacology Group, based at our research site in Braine ‘L-Alleud, Belgium, we are seeking a talented individual to fill the position of Quantitative Clinical Pharmacology Lead.You like to work in an environment where you can:Demonstrate experience in strategically leading clinical pharmacology input for large or small molecules into development programs from pre-FIH to life-cycle management.You Will Contribute By- Leading and scoping the quantitative clinical pharmacology activities in assigned project(s) to drive further Early and Late Clinical Development within UCB
- working with other functional experts to create a clinical development plan
- In collaboration with other disciplines, he/she will be accountable and responsible for leading and driving, for the assigned project(s), an integrated PK-PD strategy (safety and efficacy) from clinical candidate selection through life-cycle management, driving dose and regimen selection and drive the implementation of model informed drug development, including trial design and execution
- As a key member of quantitative discovery and development (QDD) and development sciences, you will foster and facilitate a collaborative working environment between non-clinical safety, DMPK, bioanalysis, non-clinical PK-PD, modelling and simulation to leverage key scientific and strategic input into projects
- From a development science perspective, you may also be responsible to ensure a clear development science strategy is formed and lead a matrix team covering; QCP, Modelling and Simulation, DMPK, Toxicology and Bioanalytical ensuring clear deliverables and key milestones are achieved and drive project decisions. He/she will also ensure high quality and robust input is given into development teams
- Educated to Pharm D or PhD (or equivalent) with either relevant academic or industrial experience
- You will have demonstrated experience (through examples) of participating and contributing to the development and execution of the clinical plan, with specific input and expertise in the clinical pharmacology components, including regulatory aspects (e.g briefing documents, MHRA meetings, pediatric plans, INDs, regulatory responses for labelling activities), and is able to attend regulatory meetings representing function and UCB with minimal coaching
- A strong understanding of pharmacodynamic and translational methods, experimental medicine tools, regulatory requirements, PK/PD, DMPK, population pharmacokinetic-pharmacodynamic modelling and simulation
Loading ...
Loading ...
Frist: 10-01-2026
Klicken Sie hier, um sich für einen kostenlosen Kandidaten zu bewerben
Job melden
Loading ...
ÄHNLICHE ARBEITEN
-
⏰ 06-01-2026🌏 Bree, Limburg
-
⏰ 06-01-2026🌏 Leuven, Flemish Brabant
-
⏰ 06-01-2026🌏 Oudenaarde, East Flanders
-
⏰ 06-01-2026🌏 Beersel, Flemish Brabant
Loading ...
-
⏰ 06-01-2026🌏 Tongeren, Limburg
-
⏰ 06-01-2026🌏 Antwerp City, Antwerp
-
⏰ 06-01-2026🌏 Izegem, West Flanders
-
⏰ 06-01-2026🌏 Woluwe-Saint-Pierre, Brussels Capital
Loading ...
-
⏰ 06-01-2026🌏 St. Vith, Liège
-
⏰ 06-01-2026🌏 La Louvière, Hainaut