In-house Clinical Research Associate II. The In-house CRA II provides overall support to study sites and clinical project teams engaged in clinical research studies. Solid experience in clinical resea...
read moreIn-house Clinical Research Associate II. The In-house CRA II provides overall support to study sites and clinical project teams engaged in clinical research studies. Solid experience in clinical resea...
read moreIn-house Clinical Research Associate II. The In-house CRA II provides overall support to study sites and clinical project teams engaged in clinical research studies. Solid experience in clinical resea...
read moreIn-house Clinical Research Associate II. The In-house CRA II provides overall support to study sites and clinical project teams engaged in clinical research studies. Solid experience in clinical resea...
read moreAdvanced knowledge of Clinical investigation of medical devices for human subjects - Good Clinical Practice (ISO 14155), 21 CFR Part 11, 50, 54, 812 and other applicable regulations, fundamental knowl...
read moreResponsible for providing Clinical Research support for all clinical trials. Responsible for procurement of budgets, contracts, regulatory documents, and other administrative documents as related to c...
read moreThe Senior Clinical Research Associate (CRA) will act as a liaison between BD (the study Sponsor) and the sites/clinics that conduct their assigned clinical studies. The Senior Clinical Research Assoc...
read moreResponsible for providing Clinical Research support for all clinical trials. Responsible for procurement of budgets, contracts, regulatory documents, and other administrative documents as related to c...
read moreResponsible for providing Clinical Research support for all clinical trials. Responsible for procurement of budgets, contracts, regulatory documents, and other administrative documents as related to c...
read moreResponsible for pre-clinical trial set up, initial and ongoing regulatory submission and IRB activities, subject screening and enrollment, specimen collection and transmittal, data collection and mana...
read moreIn depth knowledge of, and skill in applying, applicable clinical research regulatory requirements, i. IQVIA is a leading global provider of clinical research services, commercial insights and healthc...
read moreResponsible for pre-clinical trial set up, initial and ongoing regulatory submission and IRB activities, subject screening and enrollment, specimen collection and transmittal, data collection and mana...
read moreEverest Clinical Research ("Everest") is a full-service contract research organization (CRO) providing a broad range of expertise-based clinical research services to worldwide pharmaceutical, biotechn...
read moreEverest Clinical Research ("Everest") is a full-service contract research organization (CRO) providing a broad range of expertise-based clinical research services to worldwide pharmaceutical, biotechn...
read moreCertified Clinical Research Professional (CCRP) or other similar research accreditation preferred. The Clinical Research Associate will:. Initiation / implementation of the observational or clinical r...
read moreAs a Sr CRA you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. Primary interfaces: Provider Functional Manager, Clinical T...
read moreWe’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 as a Clinical Research Associ...
read moreWe’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 as a Clinical Research Associ...
read moreWorldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that a...
read moreWorldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that a...
read moreIQVIA is seeking a Senior Clinical Research Associate with at least 2 years of monitoring experience in one of the following therapeutic areas: Central Nervous System (CNS) or Cardiovascular/Renal/Met...
read moreIQVIA is seeking a Senior Clinical Research Associate with at least 2 years of monitoring experience in one of the following therapeutic areas: Central Nervous System (CNS) or Cardiovascular/Renal/Met...
read moreWorldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that a...
read moreWorldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that a...
read moreGood knowledge of, and skill in applying, applicable clinical research regulatory requirements (i. IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research ...
read moreIQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. Good Clinical Practice (GCP) and International Conference o...
read moreIQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. Good Clinical Practice (GCP) and International Conference o...
read moreGood knowledge of, and skill in applying, applicable clinical research regulatory requirements. IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research ser...
read morePresent scientific results in internal research meetings.
The Cancer Clinical Trials Senior Research Associate supports the research team in the overall conduct of clinical trials using Good Clinical Practice. The Senior Research Associate can function indep...
read moreThe Cancer Clinical Trials Senior Research Associate supports the research team in the overall conduct of clinical trials using Good Clinical Practice. The Senior Research Associate can function indep...
read moreThis position serves as a key role in the effective implementation of the global development strategy leading or co-leading one or more clinical trials in a therapeutic area for one or more compounds ...
read moreThis position serves as a key role in the effective implementation of the global development strategy leading or co-leading one or more clinical trials in a therapeutic area for one or more compounds ...
read moreThe Clinical Research Associate will support clinical research activities within research sites that are actively participating in clinical trials. Under the direction of the Clinical Study Manager(s)...
read moreThe Clinical Research Associate will support clinical research activities within research sites that are actively participating in clinical trials. Under the direction of the Clinical Study Manager(s)...
read moreThrough the above mentioned partnership and an academic appointment at Rutgers, The State University of New Jersey, unique opportunities exist for collaborations between clinical and research programs...
read moreThrough the above mentioned partnership and an academic appointment at Rutgers, The State University of New Jersey, unique opportunities exist for collaborations between clinical and research programs...
read moreClinical Research Associate (CRA) III. As a Clinical Research Associate (CRA) III, your responsibilities:. Strong knowledge of Good Clinical Practice (international quality standard for human clinical...
read moreClinical Research Associate (CRA) III. As a Clinical Research Associate (CRA) III, your responsibilities:. Strong knowledge of Good Clinical Practice (international quality standard for human clinical...
read moreThe Associate Director of Clinical Research will work with the MCIT leadership to be responsible for the implementation and operations of all aspects of clinical research systems for NYU Langone Healt...
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