The Associate Clinical Research III will assist in the clinical execution and management of all aspects of assigned clinical studies. Solid understanding and demonstrated experience of the clinical trial process including study design and conduct; clinical data management systems; clinical trial man...
A Senior Clinical Research Associate will work closely with clinical operations and the cross-functional study execution team to implement all aspects of clinical trials to support multiple clinical programs. Senior Clinical Research Associate. The position will liaise with clinical sites, central l...
Senior Clinical Research Associate. We are partnered with a rapidly expanding Neurology company in their search for a Senior Clinical Research Associate. This organization has already received multiple approvals for therapies generating upwards of 100 million dollars in revenue per year and they hav...
Avania is hiring Senior Clinical Research Associates (Sr CRAs) - West Coast - Extensive cardiology Class III device monitoring experience required. Avania’s ClinOps Team establishes, maintains and supports clinical trials; as a key member of the team, our Sr CRA performs clinical trial oversight for...
Job Title: Senior Research Associate, Drug Metabolism. The primary responsibility of this Biologics Bioanalytical Research Associate is to provide bioanalytical support to. ...
HJF is seeking a Senior Clinical Research Associate to monitor and facilitate the execution of a clinical program, ensure that all necessary steps are taken towards safety provisions, and all regulations are adhered to. As a project lead, the Senior Clinical Research Associate submits protocol appli...
The Lead Clinical Research Associate manages the design, execution, and monitoring of internal and external clinical studies, coordinates the development of operating procedures, coordinates in the development of standard procedures in executing experiments, evaluation, and documentation of results,...
Manage, deliver and/or perform full clinical site monitoring services for one or more projects, which may include multiple services, be complex in nature and/or run on a multinational scale. May represent Director, Monitoring and Site Management or Manager, Clinical Site Management in BD initiatives...
Senior Clinical Research AssociateA Senior Clinical Research Associate will work closely with clinical operations and the cross-functional study execution team to implement all aspects of clinical trials to support multiple clinical programs. The position will liaise with clinical sites, central lab...
The Clinical Research Associate is the clinical sites’ direct point of contact and accountable for managing site quality and delivery from site identification through close-out. The Clinical Research Associate will oversee the conduct of the trial at designated sites, ensuring the rights and well-be...
The Associate Clinical Research III will assist in the clinical execution and management of all aspects of assigned clinical studies. Solid understanding and demonstrated experience of the clinical trial process including study design and conduct; clinical data management systems; clinical trial man...
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. ...
Supporting study operational activities under the direction of the clinical study lead. ...
As a Clinical Research Associate at Parexel, you will be joining a team with a wide variety of experiences and knowledge. Your hard work may be rewarded through a bonus incentive program, the opportunity to work within multiple therapeutic areas and an opportunity to advance your career in clinical ...
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 Lead Clinical Research Associate manages the design, execution, and monitoring of internal and external clinical studies, coordinates the development of operating procedures, coordinates in the development of standard procedures in executing experiments, evaluation, and documentation of results,...
The incumbent will serve as a Staff Research Associate III/Clinical Research Coordinator for various project and will provide compliance oversight and day-to-day study coordination activities as assigned by the Manager of Compliance and Contracts. The Clinical Research Coordinator (CRC) is a special...
Ensures adherence to federal regulations and applicable local regulations, Good Clinical Practices (GCPs), ICH Guidelines, AbbVie Standard Operating Procedures (SOPs), Monitoring Plans, and to quality standards in conducting clinical research. Minimum of 1 year of clinically-related experience, of w...
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...
Under the supervision of Principal Investigator (PI), the clinical research coordinator (CRC) will perform duties related to the support and coordination of clinical research studies and may receive training and development to prepare and advance for journey-level work at the next level within the s...
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...
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...
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. ...
The Clinical Research Coordinator (CRC) will be responsible for providing clinical and administrative support to the Principal Investigator (PI) for a variety of research studies conducted in the SFVAHCS Cardiac Catheterization Laboratory (CCL). The CRC will be responsible for the coordination of on...
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. ...