Pharmacokinetics - 42+ Stellen

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. The Senior Specialist Medical Informatio

At Debiopharm, every step we take is guided by one purpose: improving the lives of people affected by cancer and infectious diseases. As a privately-owned Swiss biopharmaceutical company, we’re driven by science, but above all, by the people behind every treatment — the patients and their families.

At Debiopharm, every step we take is guided by one purpose: improving the lives of people affected by cancer and infectious diseases. As a privately-owned Swiss biopharmaceutical company, we're driven by science, but above all, by the people behind every treatment — the patients and their families.

CSL Behring

Position Description Summary: The Scientist PK is responsible for monitoring of non-clinical PK/TK studies conducted internally and externally both in a GLP and non-GLP environment and support modelling activities. Main Responsibilities: Design, oversee, and interpret nonclinical PK/QSP studies (GLP

CSL Behring

Position Description Summary: The Principal Scientist PK/QSP will lead and manage nonclinical PK/QSP strategies across multiple drug development projects. This role serves as the primary PK/QSP representative on interdisciplinary project teams and provides scientific leadership from early discovery

Description Summary: The Associate Director PK is responsible for leading the design, execution, and interpretation of pharmacokinetic (PK), toxicokinetic (TK), strategies to support drug discovery, nonclinical and development programs across multiple therapeutic areas. The Sr. Expert will lead a te

Description Summary: The Scientist PK is responsible for monitoring of non-clinical PK/TK studies conducted internally and externally both in a GLP and non-GLP environment and support modelling activities Main Responsibilities: Design, oversee, and interpret nonclinical PK/QSP studies (GLP and non-G

Description Summary: The Principal Scientist PK/QSP will lead and manage nonclinical PK/QSP strategies across multiple drug development projects. This role serves as the primary PK/QSP representative on interdisciplinary project teams and provides scientific leadership from early discovery through r

Associate Director, Pharmacokinetics (PK) page is loaded## Associate Director, Pharmacokinetics (PK)locations: EMEA, CH, Glattbrugg, CSL Behringtime type: Vollzeitposted on: Gestern ausgeschriebenjob requisition id: R- CSL's R&D organization is accelerating innovation to deliver greater impact for p

Description Summary: The Scientist PK is responsible for monitoring of non-clinical PK/TK studies conducted internally and externally both in a GLP and non-GLP environment and support modelling activities Main Responsibilities: Design, oversee, and interpret nonclinical PK/QSP studies (GLP and non-G

Description Summary: The Principal Scientist PK/QSP will lead and manage nonclinical PK/QSP strategies across multiple drug development projects. This role serves as the primary PK/QSP representative on interdisciplinary project teams and provides scientific leadership from early discovery through r

ph3Position Description Summary /h3 pThe Associate Director PK/QSP is responsible for leading the design, execution, and interpretation of pharmacokinetic (PK), toxicokinetic (TK), strategies to support drug discovery, nonclinical and development programs across multiple therapeutic areas. The Sr. E

pDescription /p Summary:pThe Principal Scientist PK/QSP will lead and manage nonclinical PK/QSP strategies across multiple drug development projects. This role serves as the primary PK/QSP representative on interdisciplinary project teams and provides scientific leadership from early discovery throu

pDescription /p Summary:pThe Associate Director PK is responsible for leading the design, execution, and interpretation of pharmacokinetic (PK), toxicokinetic (TK), strategies to support drug discovery, nonclinical and development programs across multiple therapeutic areas. The Sr. Expert will lead

Position Description Summary The Associate Director PK/QSP is responsible for leading the design, execution, and interpretation of pharmacokinetic (PK), toxicokinetic (TK), strategies to support drug discovery, nonclinical and development programs across multiple therapeutic areas. The Sr. Expert wi

pDescription /p Summary:pThe Scientist PK is responsible for monitoring of non-clinical PK/TK studies conducted internally and externally both in a GLP and non-GLP environment and support modelling activities /ppbMain Responsibilities: /b /ppDesign, oversee, and interpret nonclinical PK/QSP studies

Description Summary: The Associate Director PK is responsible for leading the design, execution, and interpretation of pharmacokinetic (PK), toxicokinetic (TK), strategies to support drug discovery, nonclinical and development programs across multiple therapeutic areas. The Sr. Expert will lead a te