If you are an experienced clinical research professional ready to take on a key role in advancing oncology research, Barrington James would love to hear from you. Professionals from academia or resear...

Certified Clinical Research Professional (CCRP) and/or Certified Clinical Research Associate (CCRA) and/or Certified Clinical Research Coordinator (CCRC). The Clinical Research Nurse is responsible fo...

If you are an experienced clinical research professional ready to take on a key role in advancing oncology research, Barrington James would love to hear from you. Clinical Research Coordinator (CRC) w...

Certified Clinical Research Professional (CCRP) and/or Certified Clinical Research Associate (CCRA) and/or Certified Clinical Research Coordinator (CCRC). The Clinical Research Nurse is responsible fo...

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...

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)...

If you are an experienced clinical research professional ready to take on a key role in advancing oncology research, Barrington James would love to hear from you. Clinical Research Coordinator (CRC) w...

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...

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 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)...

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...

If you are an experienced clinical research professional ready to take on a key role in advancing oncology research, Barrington James would love to hear from you. Clinical Research Coordinator (CRC) w...

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...

If you are an experienced clinical research professional ready to take on a key role in advancing oncology research, Barrington James would love to hear from you. Professionals from academia or resear...

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...

Responsible for coordination with clinical suppliers to ensure appropriate and timely delivery of clinical trial supplies to clinical sites. Minimum of 8 + years drug development experience in the pha...

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. Tracking of clini...

The Associate Director, Outcomes Research & RWE is responsible for executing and managing plans for outcomes research and real-world evidence programs. Master’s degree in health economics, outcomes re...

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. Tracking of clini...

Master’s degree in health economics, outcomes research, epidemiology, health services research, public health, health policy with demonstrated research accomplishments (e. The Associate Director, Outc...

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. Tracking of clini...

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. Demonstrate excellent qualifications in education, clinical care or r...

The oncology clinical research nurse I is expected to develop and maintain competencies in clinical research nursing in the first year of the position including but not limited to comprehension and co...

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...

Expertise in pharmaceutical medicine based on industry experience (2+ years) or academic clinical research experience (2+ years), preferably with experience in clinical development. Reporting to the G...

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

Experience working in a clinical research/trial participant facing role is a big plus (but this is not a requirement – resource will be trained in clinical research). Proactively manages, coordi...

Experience working in a clinical research/trial participant facing role is a big plus (but this is not a requirement – resource will be trained in clinical research). Proactively manages, coordi...

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...

IQVIA 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...

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...

Oversees clinical research staff performing clinical functions i. Leads clinical research activities within the department under the direction of a physician; exhibits technical and functional experti...

IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. Good knowledge of, and skill in applying, applicable clinic...

This 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 ...

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)...