The Clinical Research Associate I works directly with a Clinical Research Coordinator, Research Program Administrator, or Research Nurse to coordinate and/or implement the study. Works with a Clinical Research Coordinator, Research Program Administrator or Research Nurse to coordinate/implement stud...
Clinical Research Associate II will participate in clinical research teams to ensure the most effective and efficient conduct of clinical research studies by providing training, protocol interpretation, document collection and review and overall clinical trial support. Bachelor's degree in a clinica...
The Clinical Research Associate II works directly with a Clinical Research Coordinator, Research Program Administrator, or Research Nurse, or Principal Investigator to coordinate and/or implement the study and may serve as the point of contact for the external sponsors. Works with a Clinical Researc...
The selected candidates will be responsible for the teaching and training of medical students, residents, and fellows in our educational programs as well as clinical research, translational research and/or basic research. The successful candidates will interact with a wide range of translational and...
The Clinical Research Associate I works directly with a Clinical Research Coordinator, Research Program Administrator, or Research Nurse to coordinate and/or implement the study. Works with a Clinical Research Coordinator, Research Program Administrator or Research Nurse to coordinate/implement stud...
The POMDC and the fellowship program will benefit from a senior research leader in the field, with federal grants who will play an important role in teaching and research, while fostering the broader research mission of the POMDC. The successful candidate will serve as Research Lead of the establish...
Key Responsibilities:Lead business development and capture for opportunities within federal agenciesDirect and manage large clinical trials support services contracts or projectsMentor a team of clinical research professionals and foster a culture of continuous improvementRequired Qualifications:Mas...
Reporting to the Lead Clinical Research Associate, the CRA II/Sr. This role will collaborate closely with key cross-functional internal stakeholders including Clinical Operations, Medical Monitoring, Data Management, Supply Chain, and Clinical Compliance and Quality as well as external CRO and vendo...
The selected candidates will be responsible for the teaching and training of medical students, residents, and fellows in our educational programs as well as clinical research, translational research, and/or basic research. The Viterbi Family Department of Ophthalmology at UC San Diego (Department We...
Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications – from discovery to reality. ...
Good knowledge of, and skill in applying, applicable clinical research regulatory requirements (i. 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 on...
Under the supervision of the Clinical Operations Director, the Clinical Research Associate (CRA) is responsible for conducting all aspects of site monitoring for clinical research studies according to our Standard Operating Procedures (SOPs) and ICH/GCP/GLP guidelines. We are a clinical stage biotec...
The Clinical Research Associate II works directly with a Clinical Research Coordinator, Research Program Administrator, or Research Nurse, or Principal Investigator to coordinate and/or implement the study and may serve as the point of contact for the external sponsors. Works with a Clinical Researc...
Responsible for the site visits, monitoring, communication and deliverables for the assigned study sites Serves as a member of the clinical study team and is the liaison between Clinical Operations and Study Site personnel for the specific clinical projects. If you have at least 5 full years of regi...
Bachelor’s Degree (BA/BS) in life sciences and minimum of three or more years of relevant experience in clinical research or healthcare related industry, including a minimum of 2 years direct field monitoring experience, or equivalent combination of education and experience. Conducts pre-study (site...
A minimum of 12 months experience as a clinical monitor with demonstrated experience of monitoring (virtual or onsite). Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements. ...
Join Cedars-Sinai and become part of a team that is at the forefront of medical advancements! The Clinical Research Associate I (CRAI) will work directly with a Clinical Research Coordinator, Research Program Administrator, Research Nurse, or Principal Investigator to coordinate and/or implement the...
Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications – from discovery to reality. ...
Join Cedars-Sinai and become part of a team that is at the forefront of medical advancements! The Clinical Research Associate I (CRAI) will work directly with a Clinical Research Coordinator, Research Program Administrator, Research Nurse, or Principal Investigator to coordinate and/or implement the...
The Clinical Research Associate I works directly with a Clinical Research Coordinator, Research Program Administrator, or Research Nurse to coordinate and/or implement the study. Works with a Clinical Research Coordinator, Research Program Administrator or Research Nurse to coordinate/implement stud...
Senior Clinical Research Associate will participate in clinical research teams to ensure the most effective and efficient conduct of clinical research studies by providing training, protocol interpretation, document collection and review and overall clinical trial support. Bachelor’s degree in a cli...
The Clinical Research Associate I works directly with a Clinical Research Coordinator, Research Program Administrator, or Research Nurse to coordinate and/or implement the study. Works with a Clinical Research Coordinator, Research Program Administrator or Research Nurse to coordinate/implement stud...
Under the supervision of the Clinical Operations Director, the Clinical Research Associate (CRA) is responsible for conducting all aspects of site monitoring for clinical research studies according to our Standard Operating Procedures (SOPs) and ICH/GCP/GLP guidelines. We are a clinical stage biotec...
GDIT's Military Health Team is hiring a Clinical Research Associate to support clinical investigations for the Traumatic Brain Injury Center of Excellence (TBICoE) located at the Naval Medical Center (NMCSD) in San Diego, California. The Research Associate will be responsible for collection, organiz...
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 concerns associated with study delivery at sites within established protocols and portfolio under gene...