Regulatory Management Jobs in La Jolla, CA

POSITION SUMMARYYou will lead and coordinate the development of multiple studies of novel biological and small molecules for first in human (FIH) proof of mechanism (POM) early signs of efficacy (ESOE) and proof of concept (POC) studies in Oncology. You will work in close collaboration with the Glob...

.POSITION SUMMARYYou will be responsible for scientific oversight data integrity and quality of clinical trial(s) in support of the development strategy for programs within the Late-Stage Oncology portfolio.KEY RESPONSIBILITIESClinical development expert for assigned studies maintaining current scie...

POSITION SUMMARYYou will be responsible for scientific oversight data integrity and quality of clinical trial(s) in support of the development strategy for programs within the Late-Stage Oncology portfolio.KEY RESPONSIBILITIESClinical development expert for assigned studies maintaining current scien...

ROLE SUMMARY:The Manager Scientific Regulatory Strategy & Submissions is a key member of the Scientific Regulatory Strategy (SRS) Oncology Research Unit (ORU) Portfolio & Scientific Operations team responsible for leading and optimizing regulatory document management process automation and scientifi...

The Director Regulatory Program Management & Submission Strategy (RPMSS) provides comprehensive program management ensuring alignment and execution of Pfizer Oncologys regulatory strategic and operational deliverables. The Director RPMSS serves as the regulatory program operational leader ensuring a...

POSITION SUMMARYYou will lead and coordinate the development of multiple studies of novel biological and small molecules for first in human (FIH) proof of mechanism (POM) early signs of efficacy (ESOE) and proof of concept (POC) studies in Oncology. You will work in close collaboration with the Glob...

POSITION SUMMARYYou will be responsible for scientific oversight data integrity and quality of clinical trial(s) in support of the development strategy for programs within our Late-Stage Oncology portfolio.KEY RESPONSIBILITIESClinical development expert for assigned studies maintaining current scien...

POSITION SUMMARYYou will be responsible for scientific oversight data integrity and quality of clinical trial(s) in support of the development strategy for programs within our Late-Stage Oncology portfolio.KEY RESPONSIBILITIESClinical development expert for assigned studies maintaining current scien...