Clinical Research Associate: salario promedio en Beverly Hills, CA in 2024

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...

A company is looking for a Study Start-Up Clinical Research Associate (SSU CRA) to manage site selection and activation phases of clinical trials. ...

As a Clinical Research Associate I, you will work directly with a Clinical Research Coordinator, Research Program Administrator, Research Nurse, or Principal Investigator to coordinate and/or implement the study. Clinical Research Associate I - Pulmonary Research Program/Lung Institute. This role su...

A company is looking for a Clinical Research Associate to support multiple projects in the healthcare field. ...

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...

A company is looking for a Histologist - CRA I to support diagnostic studies....

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...

Clinical Research Associate (Sr. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates. Minimum of five (5) years in clinica...

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. This role evaluates and abstracts research data and ensures compliance with protocol and research objectives. The inc...

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...

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...

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...

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...

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 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. ...

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 ...

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. Working Title : Clinical Research Associate I, PER_DIEM -Heart Institute. Evaluates and abstracts research data and ensur...

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...

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 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...