Clinical Research Associate II/Sr. You will monitor and own the progress of clinical studies at investigative sites and ensure that clinical studies are conducted, recorded, and reported per protocol,...
read moreClinical Research Associate II/Sr. You will monitor and own the progress of clinical studies at investigative sites and ensure that clinical studies are conducted, recorded, and reported per protocol,...
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 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 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 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 moreClinical Research Associate II/Sr. You will monitor and own the progress of clinical studies at investigative sites and ensure that clinical studies are conducted, recorded, and reported per protocol,...
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 moreClinical Research Associate II/Sr. You will monitor and own the progress of clinical studies at investigative sites and ensure that clinical studies are conducted, recorded, and reported per protocol,...
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 Clinical Research Associate I monitors all aspects of clinical research trial(s) Clinical study life-cycle responsibilities including site management, ongoing maintenance and closure of pre-clinic...
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 moreAs a Clinical Research Associate, you will join the world’s largest and most comprehensive clinical research organization, powered by healthcare intelligence. Primary: Provider Functional Manager, Cli...
read moreAs a Clinical Research Associate, you will join the world’s largest and most comprehensive clinical research organization, powered by healthcare intelligence. Primary: Provider Functional Manager, Cli...
read moreThe Clinical Research Associate I monitors all aspects of clinical research trial(s) Clinical study life-cycle responsibilities including site management, ongoing maintenance and closure of pre-clinic...
read moreUnique opportunities exist for collaborations between clinical and research programs, including clinical trials research, cancer chemoprevention, clinical and basic pharmacology, and Phase 1 clinical ...
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 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 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 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 moreAs a Clinical Research Associate, you will join the world’s largest & most comprehensive clinical research organization, powered by healthcare intelligence. Primary interfaces include Provider Functio...
read moreAs a Clinical Research Associate, you will join the world’s largest & most comprehensive clinical research organization, powered by healthcare intelligence. Primary interfaces include Provider Functio...
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 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 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 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 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 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 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 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 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 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 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 moreEmploy product management mindset in order to ensure the successful delivery of Clinical Research products such as Clinical Research Management Systems, Clinical Trials Management Systems, EDC (Electr...
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