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...
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...
The Clinical Research Associate I plays a vital role in the success of our research initiatives at Cedars-Sinai Medical Center. This position is responsible for coordinating and implementing clinical trials, ensuring compliance with protocol and research objectives. Evaluates and abstracts 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...
Minimum one (1) year of training and/or experience in research methodology/research study design, hypothesis testing; ORMinimum one (1) year of experience in clinical trials protocols involving research methodology/research study design, and hypothesis testing; ORMinimum one (1) year experience in h...
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...
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 I works directly with a Clinical Research Coordinator, Research Program Administrator, or Research Nurse to coordinate and/or implement the study. Primary Duties and Responsibilities • Works with a Clinical Research Coordinator, Research Program Administrator or Resea...
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...
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 Data Associate III manages the data for assigned research studies. In addition, may supervise clinical research staff or clinical data managers, perform sophisticated statistical analysis, and work with bioinformatics to develop and maintain trial management and validation syst...
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...
Join our team and use your skills 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. Req ID : HRC1284584A ...
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 and Responsibilities• Works with a Clinical Research Coordinator, Research Program Administrator or Resear...
We are a national staffing firm and are currently seeking a Clinical Research Associate for a prominent Medical Device client of ours. Support clinical activities to stay in compliance with the study Monitoring Plan requirements and compliance to Protocol, applicable regulatory standards, IRB polici...
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 (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...
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...
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 will work 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 - Karsh Division of Gastroenterology and Hepatology (Per Diem). This ro...
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...
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...
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...