P2621 - (Senior) Pharmacometrician — Debiopharm
- Location
- Lausanne
- Contract
- other
- Posted
- 19 days ago
Role overview
At Debiopharm you will be at the forefront of the fight against cancer and infectious diseases, and you will have the opportunity to work on new innovative medicines for patients.
Efficacy is our mode of action, saving lives our collective target.
In this role, you will contribute to the modeling and simulation activities for projects in Oncology and Antibiotics, leveraging state-of-the-art PK,PK/PD and other methodologies.
- At Debiopharm you will be at the forefront of the fight against cancer and infectious diseases, and you will have the opportunity to work on new innovative medicines for patients.
- Efficacy is our mode of action, saving lives our collective target.
- Your responsibilities will be but not limited to: Requirements
- PhD or equivalent degree in Pharmacometrics, mathematics, statistics, or similar disciplines with demonstrated expertise in pharmacometrics (e.g., population PK and PK/PD modeling, exposure-response analysis, disease progression models, clinical trial simulation)
- At least 3-5 years relevant experience in PMx within industry or academia; experience in oncology is an asset
- International, highly dynamic environment with a long-term vision.
Main responsibilities
- Your responsibilities will be but not limited to: Requirements
- PhD or equivalent degree in Pharmacometrics, mathematics, statistics, or similar disciplines with demonstrated expertise in pharmacometrics (e.g., population PK and PK/PD modeling, exposure-response analysis, disease progression models, clinical trial simulation)
- At least 3-5 years relevant experience in PMx within industry or academia; experience in oncology is an asset
- Solid hands-on experience in Population PK/PD modelling software (Monolix, NONMEM);
- Excellent programming skills (R, Python, …);KnowledgeKnowledge of PBPK modeling software (e.g.: SimCYP, PK-Sim, Gastro-Plus) is an asset.
- In depth understanding of pharmacology and pharmacokinetic concepts, as well as knowledge of preclinical and clinical development.
- Knowledge of GCP, GCLP and relevant regulatory guidelines.
- Ability to work independently in a fast-paced environment while maintaining strong collaborations both within and cross functions.
Key requirements
- PhD or equivalent degree in Pharmacometrics, mathematics, statistics, or similar disciplines with demonstrated expertise in pharmacometrics (e.g., population PK and PK/PD modeling, exposure-response analysis, disease progression models, clinical trial simulation)
- At least 3-5 years relevant experience in PMx within industry or academia; experience in oncology is an asset
- Solid hands-on experience in Population PK/PD modelling software (Monolix, NONMEM); Excellent programming skills (R, Python, …);KnowledgeKnowledge of PBPK modeling software (e.g.: SimCYP, PK-Sim, Gastro-Plus) is an asset.
- In depth understanding of pharmacology and pharmacokinetic concepts, as well as knowledge of preclinical and clinical development.
- Knowledge of GCP, GCLP and relevant regulatory guidelines.
- Ability to work independently in a fast-paced environment while maintaining strong collaborations both within and cross functions.
- Strong organizational skills and ability to handle multiple tasks simultaneously.
- Results interpretation capabilities, strong scientific/technical wring/reporting abilities, and interpersonal skills in English, French is an asset.
What the company offers
- International, highly dynamic environment with a long-term vision.
- Cross-functional collaboration at the forefront of the most advanced scientific developments in oncology and anti-bacterial industry
- Exposure to a wide variety of areas and functions within clinical development and the pharmaceutical industry
- Opportunity of personal development through specific trainings and attendance to scientific conferences
- Participation in a company where innovation, people and entrepreneurship are the fundamental keys to success.
- Proud to be an Equal-Pay certified, we ensure offering to all our employees the same opportunities
Company and context
- Strong organizational skills and ability to handle multiple tasks simultaneously.
- Results interpretation capabilities, strong scientific/technical wring/reporting abilities, and interpersonal skills in English, French is an asset.
Additional details
- Your responsibilities will be but not limited to:
Notes and original content
- Requirements
Questions about this listing
What salary does Debiopharm offer for this role?
Debiopharm lists CHF 83'500 - 126'500 gross per year for this position in Lausanne. This is the salary published in the original listing (or, when the employer omits a figure, a realistic estimate for the role and sector) — the calculator on this site converts it to your actual net take-home once cross-border tax and social contributions are applied.
Is this a full-time role, and what type of contract does Debiopharm offer?
This listing is a full-time position. The contract type shown here comes directly from the employer's original posting; always confirm exact hours, notice period and probation length with Debiopharm during the application process, since these details can vary by role even within the same contract category.
Do I need a cross-border work permit for a role in Vaud?
EU/EFTA residents living in the border zone of the country adjoining Canton Vaud can apply for a G permit; the Swiss employer files it with that canton's migration office after the contract is signed. Border-zone rules and processing times vary by neighbouring country and canton, so confirm the specifics with Vaud's cantonal migration office or with HR during the application.
How do I apply for this position at Debiopharm?
Use the "Apply now" button on this page — it links directly to Debiopharm's original listing at apply.workable.com, so your application goes straight to the employer's own applicant-tracking system. Frontaliere Ticino does not collect or forward applications itself.
