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...
A company is looking for a Clinical Research Associate in Oncology. ...
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...
A company is looking for a Senior Clinical Research Associate. Key Responsibilities:Conduct site monitoring visits in accordance with regulatory requirementsManage progress of assigned studies by tracking regulatory submissions and approvalsCreate and maintain documentation regarding site management...
From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do. Parexel Early Phase Clinical Unit. Glendale, CA Early Phase Clinical Unit (candidates must be local to Glendale, CA...
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...
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 ...
Minimum two (2) years of experience in clinical protocols involving research methodology/research study design, and hypothesis testing. May coordinate research project activities with other research study centers. If assigned to clinical trial, may work with Sponsors/ monitors at clinical sites. Min...
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...
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 Trial Assistant, Local Trial Manager and Central Study Team for assigned clinical trials. Have a mini...
Join our team and use your experience with an organization known nationally for excellence in research! 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. Primary Duties an...
Los Angeles in clinical research, promote effective education, training and career development for faculty and staff engaged in clinical research to ensure safe and quality research conduct, work with other research leaders to promote partnerships between basic and clinical researchers and between c...
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 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 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...
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...
Title: Clinical Research Associate. REQUIRED EXP: Min yrs exp in a clinical research coordinator role with recent experience being in an Academic Medical Center. ...
The Clinical Research Associate I 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. Clinical Research Coordinat...
Job Description 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. Jobs-Indeed R...
RDI is seeking a Senior Clinical Associate to ensure our clinical trials are completed on-time, according to the protocol, and keeping our clients and sites informed throughout the process. A minimum of 2 years clinical research experience (either as a high-achieving research coordinator or CRA). Kn...
Minimum one (1) year of experience in clinical trials protocols involving research methodology/research study design, and hypothesis testing; OR. If assigned to clinical trial, may work with Sponsors/ monitors at clinical sites. Minimum one (1) year of training and/or experience in research methodol...
REQUIRED EXP: Min yrs exp in a clinical research coordinator role with recent experience being in an Academic Medical Center. ...
Provide oversight of clinical research sites compliance with ICH/Good Clinical Practices (GCP), governing SOPs (standard operating procedures) and clinical study protocols. Clinical Research Associate 2580199. Responsible for regulatory coordination of clinical research studies, preparation, submiss...
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. ...