Regulatory Documents Jobs in La Jolla, CA

.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...

Use Your Power for PurposeYou will have a profound impact on improving patients lives by ensuring our evidence is scientifically robust and providing unbiased medically essential expertise. Your role is vital in connecting sound scientific evidence with practical medical insights to enhance health a...

Use Your Power for PurposeYou will have a profound impact on improving patients lives by ensuring our evidence is scientifically robust and providing unbiased medically essential expertise. Your role is vital in connecting sound scientific evidence with practical medical insights to enhance health a...

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 SUMMARYThe Global Medical Strategy and Team Lead Seasonal & Viral Pipeline Vaccines is responsible for designing and overseeing execution of the medical strategies leading to the licensure and public health implementation of seasonal vaccines in their portfolio. The portfolio includes COVID-19...

The Global Medical Strategy and Team Lead Seasonal & Pipeline Viral Vaccines is responsible for designing and overseeing execution of the medical strategies leading to the licensure and public health implementation of seasonal vaccines in their portfolio. The portfolio includes COVID-19 vaccines com...

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...

Use Your Power for Purpose This position is for a Senior Medical Director within the hematology program. This individual contributor position will be responsible for supporting clinical trial(s) and lead subteams in clinical development. The successful candidate should ideally have prior experience...

Use Your Power for Purpose This position is for a Senior Medical Director within the hematology program. This individual contributor position will be responsible for supporting clinical trial(s) and lead subteams in clinical development. The successful candidate should ideally have prior experience...

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...

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...