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...
A company is looking for a Histologist - CRA I to support diagnostic studies....
The Clinical Research Associate I will work directly with a Clinical Research Coordinator, Research Program Administrator, or Research Nurse to coordinate and/or implement the study. Clinical Research Associate I - Karsh Division of Gastroenterology and Hepatology (Per Diem). This role evaluates and...
Drives the understanding and delivery of quality clinical research (patient safety, rights and wellbeing; data reliability; scientific integrity; regulatory and process compliance) for monitoring and site management activities. Takes ownership to deliver upon near-term North America Clinical Develop...
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...
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...
REQUIRED EXP: Min yrs exp in a clinical research coordinator role with recent experience being in an Academic Medical Center. ...
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...
Key Job Responsibilities: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. Working Title : Clinical Research Associate I - Heart Institute. Evaluates and abstracts researc...
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 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 Clinical Research Data Associate II manages the data for assigned research studies. In addition, may train clinical research staff, perform basic statistical analysis, and work with bioinformatics to develop and maintain trial management systems. May train clinical research staff to help improve...
Bachelors degree with 4+ year experience as a Clinical Trials Associate; or Associate’s degree with 7+ years’ experience as a Clinical Trials Associate; or 10+ years clinical research experience. Participate in clinical research teams to ensure the most effective and efficient conduct of clinical re...
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. ...
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 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...
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...
Title: Clinical Research Associate. REQUIRED EXP: Min 2 yrs exp in a clinical research coordinator role with recent experience being in an Academic Medical Center. ...
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...
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...
Drives the understanding and delivery of quality clinical research (patient safety, rights and wellbeing; data reliability; scientific integrity; regulatory and process compliance) for monitoring and site management activities. Takes ownership to deliver upon near-term North America Clinical Develop...
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 ...
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 ...