Syndax Pharmaceuticals is looking for a Senior Clinical Research Associate (in-house). Perform a key role in building relationships with site Clinical Coordinators, Study Investigators, and Service Pr...
read moreSyndax Pharmaceuticals is looking for a Senior Clinical Research Associate (in-house). Perform a key role in building relationships with site Clinical Coordinators, Study Investigators, and Service Pr...
read moreSyndax Pharmaceuticals is looking for a Clinical Research Associate. Perform a key role in building relationships with site Clinical Coordinators, Study Investigators, and Service Provider partners an...
read moreIn addition to those duties expected of an Associate Research Technician, Research Technicians may be expected to coordinate the repair and preventive maintenance of lab equipment. Maintains the confi...
read moreIn addition to those duties expected of an Associate Research Technician, Research Technicians may be expected to coordinate the repair and preventive maintenance of lab equipment. Maintains the confi...
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 moreThe position arranges and oversees all clinical trial activities and plays a key role in assisting the Principal Investigator (PI) in recruiting patients for clinical studies. Combining state-of-the-a...
read moreThe position arranges and oversees all clinical trial activities and plays a key role in assisting the Principal Investigator (PI) in recruiting patients for clinical studies. Combining state-of-the-a...
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 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 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 moreAt least 2 years' experience as a Clinical Research Associate with a sound track record in managing clinical trial sites. Maintain current knowledge related to cancer therapy, clinical trial design an...
read moreThe Non-therapeutic Oncology Associate Clinical Research Coordinator (NT aCRC) is an active participant in the coordination of oncology clinical research studies from research planning and throughout ...
read moreAt least 2 years' experience as a Clinical Research Associate with a sound track record in managing clinical trial sites. Maintain current knowledge related to cancer therapy, clinical trial design an...
read moreThe Non-therapeutic Oncology Associate Clinical Research Coordinator (NT aCRC) is an active participant in the coordination of oncology clinical research studies from research planning and throughout ...
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 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 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 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 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 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 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 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 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 moreThe Clinical Research Associate will:. Initiation / implementation of the observational or clinical research projects assigned including: Maintenance of Investigator and Research Staff CVs, Licensure ...
read moreThe Clinical Research Associate will:. Initiation / implementation of the observational or clinical research projects assigned including: Maintenance of Investigator and Research Staff CVs, Licensure ...
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 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 moreThe aCRC supports the management of the research biospecimen/biofluid components of clinical research studies, performs accurate execution of research protocols in accordance with PCC CTO Research Bio...
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 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 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...
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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