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...
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...
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 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 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, PER_DIEM -Heart Institute. Evaluates and abstracts research data and ensur...
The Clinical Research Associate II will work directly with a Clinical Research Coordinator, Research Program Administrator, Research Nurse, or Principal Investigator to coordinate and/or implement the study and may serve as the point of contact for external sponsors. Lisa Bateman, MD is seeking a hi...
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. ...
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 Associate II. Participates in global clinical monitoring/project staff meetings (inclusive of Sponsor representation, as applicable) and attends clinical training sessions according to the project specific requirements. We translate unique clinical, medical affairs and commercial i...
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 ...
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...
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...
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 under the direction of a Clinical Research Coordinator, Research Program Administrator, Research Nurse, or other supervising staff to assist in tasks supporting the coordination/implementation of noncomplex research studies. Works under the direction of a Clin...
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...
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 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 (CRA) is responsible for establishing and maintaining the Study Master File, tracks critical trial information, and supports Regional Clinical Research Associates under the guidance of a Clinical Manager or Clinical Director. Obtains site documents from Regional Clini...
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...
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 Department of Medicine Clinical Trial Program is seeking a skilled Clinical Research Associate to oversee, manage and participate in research activities. Providing oversight of clinical research sites compliance with ICH/Good Clinical Practices (GCP), governing SOPs (standard operating procedure...
The Accelerated Program of Education, Exposure, and Experience for Clinical Research Associates (APEX CRA) provides foundational clinical research training including project and system experience. Do you have up to 2 years of experience working as a Clinical Research Coordinator in Ophthalmology or ...
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...