Dein persönlicher KI-Karriere-Agent
Principal Clinical Pharmacologist(m/w/x)
Designing clinical pharmacology studies for oncology/infectious diseases, including SAD/MAD PK and drug-drug interactions. PhD in life sciences or related discipline required. International and dynamic environment.
Anforderungen
- PhD (PharmD is a plus) in Life sciences, pharmacokinetics, clinical pharmacology, or related discipline
- Expertise in Non-Compartmental PK analysis, Population PK/PD, Modeling & Simulation
- Excellence knowledge of GCP, GCLP, GLP, and relevant regulatory guidelines
- Experience in Antibody Drug Conjugate development is an asset
- Working in cross-functional teams and fast-paced environments
- Team player, tackling challenges together with team
- Excellent communication skills in English (oral and written)
- Doctorate education
Aufgaben
- Lead clinical pharmacology strategy for Oncology/Infectious diseases projects
- Manage clinical pharmacology activities for assigned projects
- Supervise clinical pharmacology activities to accelerate medicine development
- Collaborate with project teams on clinical pharmacology strategy
- Design clinical pharmacology studies (SAD/MAD PK, bioequivalence, food effect, drug-drug interactions, PK in special populations)
- Develop pharmacometrics strategy with pharmacometricians
- Organize pharmacometrics activities for assigned projects
- Contribute to clinical trial protocols
- Manage PK and PK/PD analyses (noncompartmental and modeling)
- Manage reporting of PK and PK/PD analyses
- Manage risk of food-drug and drug-drug interactions
- Manage outsourced activities from provider selection to completion
- Prepare clinical pharmacology and pharmacometrics documentation for regulatory support
- Participate in Health Authority interactions
- Contribute to scientific communication and events
- Contribute to In & Out licensing activities
- Contribute to external fund-raising activities
Berufserfahrung
- 7 Jahre
Ausbildung
- Doktor / Ph.D.
Sprachen
- Englisch – verhandlungssicher
- Französisch – Grundkenntnisse
Tools & Technologien
- Non-Compartmental PK analysis
- Population PK/PD
- Modeling & Simulation
- GCP
- GCLP
- GLP
Benefits
Lockere Unternehmenskultur
- International and dynamic environment
Noch nicht perfekt?
- Isomorphic LabsVollzeitnur vor OrtSeniorLausanne
- Debiopharm
Associate Safety Physician(m/w/x)
Vollzeitnur vor OrtBerufserfahrenLausanne - Isomorphic Labs
Chemistry Lead (Induced Proximity)(m/w/x)
Vollzeitnur vor OrtSeniorLausanne - Société des Produits Nestlé S.A.
Medical Director Safety(m/w/x)
Vollzeitnur vor OrtSeniorLausanne - SUSONITY
Process Validation Expert(m/w/x)
Vollzeitnur vor OrtSeniorAubonne
Principal Clinical Pharmacologist(m/w/x)
Designing clinical pharmacology studies for oncology/infectious diseases, including SAD/MAD PK and drug-drug interactions. PhD in life sciences or related discipline required. International and dynamic environment.
Anforderungen
- PhD (PharmD is a plus) in Life sciences, pharmacokinetics, clinical pharmacology, or related discipline
- Expertise in Non-Compartmental PK analysis, Population PK/PD, Modeling & Simulation
- Excellence knowledge of GCP, GCLP, GLP, and relevant regulatory guidelines
- Experience in Antibody Drug Conjugate development is an asset
- Working in cross-functional teams and fast-paced environments
- Team player, tackling challenges together with team
- Excellent communication skills in English (oral and written)
- Doctorate education
Aufgaben
- Lead clinical pharmacology strategy for Oncology/Infectious diseases projects
- Manage clinical pharmacology activities for assigned projects
- Supervise clinical pharmacology activities to accelerate medicine development
- Collaborate with project teams on clinical pharmacology strategy
- Design clinical pharmacology studies (SAD/MAD PK, bioequivalence, food effect, drug-drug interactions, PK in special populations)
- Develop pharmacometrics strategy with pharmacometricians
- Organize pharmacometrics activities for assigned projects
- Contribute to clinical trial protocols
- Manage PK and PK/PD analyses (noncompartmental and modeling)
- Manage reporting of PK and PK/PD analyses
- Manage risk of food-drug and drug-drug interactions
- Manage outsourced activities from provider selection to completion
- Prepare clinical pharmacology and pharmacometrics documentation for regulatory support
- Participate in Health Authority interactions
- Contribute to scientific communication and events
- Contribute to In & Out licensing activities
- Contribute to external fund-raising activities
Berufserfahrung
- 7 Jahre
Ausbildung
- Doktor / Ph.D.
Sprachen
- Englisch – verhandlungssicher
- Französisch – Grundkenntnisse
Tools & Technologien
- Non-Compartmental PK analysis
- Population PK/PD
- Modeling & Simulation
- GCP
- GCLP
- GLP
Benefits
Lockere Unternehmenskultur
- International and dynamic environment
Über das Unternehmen
Debiopharm
Branche
Pharmaceuticals
Beschreibung
Debiopharm is a privately-owned Swiss biopharmaceutical company committed to research in oncology and infectious diseases to improve patient outcomes and quality of life.
Noch nicht perfekt?
- Isomorphic Labs
Team Leader / Research Leader (Computational Drug Design)(m/w/x)
Vollzeitnur vor OrtSeniorLausanne - Debiopharm
Associate Safety Physician(m/w/x)
Vollzeitnur vor OrtBerufserfahrenLausanne - Isomorphic Labs
Chemistry Lead (Induced Proximity)(m/w/x)
Vollzeitnur vor OrtSeniorLausanne - Société des Produits Nestlé S.A.
Medical Director Safety(m/w/x)
Vollzeitnur vor OrtSeniorLausanne - SUSONITY
Process Validation Expert(m/w/x)
Vollzeitnur vor OrtSeniorAubonne