Responsible 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...

As a specialized research professional the Senior Clinical Research Associate (SrCRA) collaborates with the Principal Investigator (PI) in leading all activity associated with research study protocols...

Responsible 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...

The 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...

Responsibilities of the Senior Clinical Research Associate / CRA II:. Qualifications of the Senior Clinical Research Associate / CRA II:. Compensation for the Senior Clinical Research Associate / CRA ...

As a specialized research professional the Senior Clinical Research Associate (SrCRA) collaborates with the Principal Investigator (PI) in leading all activity associated with research study protocols...

As a specialized research professional the Senior Clinical Research Associate (SrCRA) collaborates with the Principal Investigator (PI) in leading all activity associated with research study protocols...

As a specialized research professional the Senior Clinical Research Associate (SrCRA) collaborates with the Principal Investigator (PI) in leading all activity associated with research study protocols...

Clinical Research; 3 years of experience in Phase I-IV clinical studies as a clinical trial assistant or clinical research associate is required. The Clinical Research Associate is an integral part of...

Masters degree or equivalent in clinical research business administration health care administration or related discipline 4 years of progressively responsible related experience coordinating clinical...

Minimum of 8 + years drug development experience in the pharmaceutical industry/CRO or commensurate clinical/medical research experience with emphasis on Phase II-IV clinical trials. Responsible for c...

Tracking of clinical data, regulatory documents, and patient enrollment information and data resolutions to assure the timely completion of clinical studies in line with approved clinical development ...

Tracking of clinical data, regulatory documents, and patient enrollment information and data resolutions to assure the timely completion of clinical studies in line with approved clinical development ...

Tracking of clinical data, regulatory documents, and patient enrollment information and data resolutions to assure the timely completion of clinical studies in line with approved clinical development ...

Academic Scholar – Clinical or Research Assistant, Associate or Full Professor, Department of Pediatrics, Division of Neonatology. Evidence of continued excellence in clinical practice, such as innova...

Academic Scholar – Clinical or Research Assistant, Associate or Full Professor, Department of Pediatrics, Division of Neonatology. Evidence of continued excellence in clinical practice, such as innova...

The 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...

The 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...

Responsible 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...

Responsible 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...

Certified Clinical Research Professional (CCRP) or other similar research accreditation preferred. The Clinical Research Associate will:. Initiation / implementation of the observational or clinical r...

Works with Clinical Trial Oversight Managers (CTOMs) and Clinical Study Team (CST) to manage site trends through dashboard review and ongoing risk assessment to ensure quality standards and address co...

Works with Clinical Trial Oversight Managers (CTOMs) and Clinical Study Team (CST) to manage site trends through dashboard review and ongoing risk assessment to ensure quality standards and address co...

As 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...

As 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...

We’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...

As a CRA you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. Ability to work effectively with investigators and other resea...

Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that a...

Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that a...

Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that a...

IQVIA 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...

Good 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...

Present 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...

The 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)...

Through 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...

Through 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...

Clinical 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...

Clinical 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...

The 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...