To achieve these goals, the Program participates in numerous industry-sponsored Phase II and III clinical trials and investigator-initiated studies. The Clinical Research Coordinator (CRC) II position...

To achieve these goals, the Program participates in numerous industry-sponsored Phase II and III clinical trials and investigator-initiated studies. The Clinical Research Coordinator (CRC) II position...

Investigator-Initiated Clinical Trials (IICTs)/Clinical Research Sponsor Collaboration (CRSC) within the organization. Design and implement a structured training curriculum tailored to various roles w...

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)...

The Clinical Research Coordinator’s primary responsibilities are to utilize Good Clinical Practices (GCPs) in the process of screening, enrolling and closely monitoring clinical research study subject...

The Clinical Research Coordinator’s primary responsibilities are to utilize Good Clinical Practices (GCPs) in the process of screening, enrolling and closely monitoring clinical research study subject...

The Clinical Research Coordinator II acts as a liaison between principal investigators, sub-investigators, clinical research nurses, and regulatory specialists on all regulatory issues and changes wit...

Everest 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...

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 I monitors all aspects of clinical research trial(s) Clinical study life-cycle responsibilities including site management, ongoing maintenance and closure of pre-clinic...

At least 4 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...

The Senior Clinical Research Associate (CRA) will act as a liaison between Ferring (the study Sponsor) and the sites/clinics that conduct their assigned clinical studies. Ensure site(s) maintains an a...

KBW is hiring for an Associate II on its Equity Research team covering Brokers, Asset Managers, and Exchanges. Develop written product with modest direction from the senior level Research Analyst. Min...

The Clinical Research Coordinator II (CRC II) is primarily responsible for coordinating the operational aspects of ongoing clinical projects to ensure that the clients' goals of time, cost, and qualit...

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...

Work with Clinical Operations Manager, study teams, and Clinical Research Organizations (CROs) to support clinical study activities as defined by the clinical trial operating model. The remote-based 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...

Work with Clinical Operations Manager, study teams, and Clinical Research Organizations (CROs) to support clinical study activities as defined by the clinical trial operating model. The remote-based C...

Main duties involve recruiting and screening research participants and running them in psychological experiments both in and out of an MRI scanner. Carry out extensive recruitment of patients for rese...

A Clinical Research Coordinator II position is currently available within the Medicine Clinical Trials Office. Determine effective strategies for recruiting research participants and retaining partici...

The Research Associate II will be an integral part of the research team. In addition, the Research Associate develops relationships with persons outside the University community to build research part...

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...

Everest 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...

Must be able to handle basic question from Sales and Clients and is beginning to represent the associates in internal research presentations. Stifel is home to approximately 9,000 individuals who are ...

An opportunity is available for a Contracts Associate II to join a Research Contracting team, providing support and advice to scientific and research leaders and contributing to the overall mission of...

An opportunity is available for a Contracts Associate II to join a Research Contracting team, providing support and advice to scientific and research leaders and contributing to the overall mission of...

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...

Rutgers, the State University of New Jersey, is seeking a Research Associate II (Research Coordinator) for the Medicine Department at NJMS- Infectious Disease. Under the direction of the Principal Inv...

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...

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. In depth knowledge of, and skill in ap...

Organization / Division / Department: Research & Development/Global Development and Clinical Safety/Global Clinical Trial Operations. Under the direction of the Director, Study Management, the Clinica...

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...

Legend Biotech is a clinical stage biopharmaceutical company focused on the discovery and development of novel cell therapies for oncology, immunology and infectious disease indications.

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...

Through the practice of professional nursing the Oncology Clinical Research Nurse (CRN) II prioritizes and advocates for the best interest of the patient enrolled on an oncology clinical trial while m...

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)...

Unique opportunities exist for collaborations between clinical and research programs, including clinical trials research, cancer chemoprevention, clinical and basic pharmacology, and Phase 1 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...