Pediatric Neonatology Research -Clinical X Series, Associate or Professor Rank. The full-time academic appointment may be at the Associate, or Full Professor level in the Clinical X series, depending on experience and extent of research effort. See Professorial Series (Adjunct, Clinical X, HS Clinic...
A company is looking for a Senior Clinical Research Associate responsible for monitoring clinical trials and ensuring compliance with regulatory standards. ...
As a CRA you will be joining the world’s largest & most comprehensive clinical research organization, powered by healthcare intelligence. Primary interfaces: Provider Functional Manager, Clinical Trial Assistant, Local Trial Manager and Central Study Team for assigned clinical trials. Have a minimum...
A company is looking for a Clinical Research Associate - Oncology. ...
If you are an experienced regional CRA looking to join a global leader in clinical research with a reputable sponsor aligned program, this is a good time to apply with ICON PLC. Primary interfaces: Provider Functional Manager, Clinical Trial Assistant, Local Trial Manager and Central Study Team for ...
As a Clinical Research Associate you will be responsible for a variety of monitoring tasks and you will have a chance to work on clinical studies in different therapeutic indications, ensuring the clinical trial is conducted in compliance with study protocol and procedures, ICH-GCP guidelines and th...
As a Clinical Research Associate focused on medical devices, you will play a crucial role in the planning, execution, and monitoring of clinical trials. You will ensure that studies are conducted in accordance with regulatory requirements, Good Clinical Practice (GCP), and company policies. Assist i...
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 Clinical Research Associate is responsible for clinical studies, site management and compliance monitoring of assigned clinical projects undertaken in support of a given product line or marketing initiative. Plan, implement and conclude clinical studies in support of project timelines/market rel...
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...
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 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...
Clinical research experience from a sponsor. Good computer skills in usage of MS Office Suite and Clinical Systems such as CTMS (Clinical Trial Management System), eTMF (electronic Trial Master file) preferred. We generate extensive clinical evidence to demonstrate the effectiveness and safety of ou...
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. ...
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 campus has produced five Nobel laureates and is known for its academic achievement, premier research, innovation and anteater mascot. The Department of Pathology & Laboratory Medicine at UC Irvine Health School of Medicine is dedicated to the diagnosis and understanding of human diseases through...
Under the direction of the Principal Investigator and Program Manager, the Assistant Clinical Research Coordinator supports the research efforts of several research projects, including regional projects and national clinical trials with the opportunity to interface with local and national level lead...
Under the supervision of the Clinical Research Manager (CRM) within the Clinical Trials Unit, the Senior Clinical Research Coordinator (SCRC) supports the clinical research efforts of the Cancer Center by providing comprehensive coordination and data management for complicated Phase I-IV cancer prot...
Under the supervision of the Clinical Research Manager and the Assistant Director of Clinical Research Operations, the incumbent is responsible for coordinating clinical trials in the UCI Center for Clinical Research (CCR). The campus has produced five Nobel laureates and is known for its academic a...
Under supervision of the Clinical Research Manager of the Clinical Trials Unit, the Assistant Clinical Research Coordinator supports the clinical research efforts of the Cancer Center by providing comprehensive coordination and data management of multiple Phase II-IV cancer-related protocols accordi...
Under the general supervision of the Principal Investigator (PI), the Clinical Research Coordinator (CRC) will be responsible for supporting the research efforts of the PI's health equity-focused Skills-based Educational Strategies to Reduce Vascular Events in Orange County (SERVE OC) family hyperte...
Under the supervision of the Assistant Director of Clinical Research Operations, the incumbent is responsible for coordinating clinical trials in the UCI Center for Clinical Research (CCR). The UCI Center for Clinical Research (CCR) is driven to improve health and wellness of people in Orange County...
A company is looking for a Customer Experience Research Associate to lead research projects focused on optimizing government services. ...