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Director, Oncology Early-Stage Clinical Scientist
PfizerSan Diego
POSITION SUMMARY You 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
Director, Oncology Early-Stage Clinical Scientist
PfizerCollegevillePOSITION SUMMARY You 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
Director, Oncology Early-Stage Clinical Scientist
PfizerSouth San FranciscoPOSITION SUMMARY You 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
Oncology Early Stage Clinical Scientist (Director, Non-MD)
PfizerCambridgePOSITION SUMMARY You 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
Oncology Late-Stage Clinical Scientist (Director, Non MD)
PfizerCambridge. POSITION SUMMARY You 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 Oncolog
Oncology Late Stage Clinical Scientist (Senior Manager, Non MD)
PfizerCambridgePOSITION SUMMARY You 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 Oncolog
Oncology Early Stage Clinical Scientist (Director, Non-MD)
PfizerNew YorkPOSITION SUMMARY You 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
Oncology Early Stage Clinical Scientist (Director, Non-MD)
PfizerGrotonPOSITION SUMMARY You 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
Oncology Late-Stage Clinical Scientist (Director, Non MD)
PfizerGroton. POSITION SUMMARY You 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 Oncolog
Oncology Late-Stage Clinical Scientist (Director, Non MD)
PfizerSan Diego. POSITION SUMMARY You 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 Oncolog
Late Stage Oncology Clinical Scientist (Director, Non MD) Multiple Positions
PfizerBothellPOSITION SUMMARY You 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
Late Stage Oncology Clinical Scientist (Director, Non MD) Multiple Positions
PfizerGrotonPOSITION SUMMARY You 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
Oncology Late-Stage Clinical Scientist (Director, Non MD)
PfizerCollegeville. POSITION SUMMARY You 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 Oncolog
Late Stage Oncology Clinical Scientist (Director, Non MD) Multiple Positions
PfizerCollegevillePOSITION SUMMARY You 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
Oncology Late Stage Clinical Scientist (Senior Manager, Non MD)
PfizerNew YorkPOSITION SUMMARY You 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 Oncolog
Oncology Late Stage Clinical Scientist (Senior Manager, Non MD)
PfizerSouth San FranciscoPOSITION SUMMARY You 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 Oncolog
Oncology Late Stage Clinical Scientist (Senior Manager, Non MD)
PfizerSan DiegoPOSITION SUMMARY You 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 Oncolog
Oncology Late Stage Clinical Scientist (Senior Manager, Non MD)
PfizerBothellPOSITION SUMMARY You 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 Oncolog
Oncology Late Stage Clinical Scientist (Senior Manager, Non MD)
PfizerSan DiegoPOSITION SUMMARY You 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 Oncolog
Oncology Late Stage Clinical Scientist (Senior Manager, Non MD)
PfizerSouth San FranciscoPOSITION SUMMARY You 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 Oncolog
Director, Oncology Scientific Communications
PfizerGrotonROLE SUMMARY Today, Pfizer Oncology has an industry-leading portfolio of 25 approved innovative cancer medicines, including major therapies for metastatic breast cancer, prostate cancer, urothelial c
Director, Oncology Scientific Communications
PfizerSan DiegoROLE SUMMARY Today, Pfizer Oncology has an industry-leading portfolio of 25 approved innovative cancer medicines, including major therapies for metastatic breast cancer, prostate cancer, urothelial c
Clinical Scientist
InderoMontreal
The Clinical Scientist is responsible for medical writing activities at Innovaderm. The individual will author or contribute to development of clinical and regulatory documents (synopsis, study protoc
