A company is looking for a Study Start-Up Clinical Research Associate (SSU CRA) to manage site selection and activation phases of clinical trials.
Key ResponsibilitiesCollaborate with teams to identify and activate clinical trial sitesPrepare and manage regulatory submissions and start-up documentationTrack and manage essential documents to ensure timely site activationRequired QualificationsBachelor's degree in life sciences, nursing, or a related fieldAt least 2 years of experience in Site Selection Visits and Study Start-Up activitiesExperience with Informed Consent Forms (ICF) review is desiredKnowledge of ICH-GCP guidelines and local regulatory requirementsStrong organizational skills with a focus on timelines and deliverables
Clinical Research Associate II - Cardiology - Towers
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. Provides limited patient cont...
Oncology Clinical Research Associate
A company is looking for a Clinical Research Associate - Oncology. ...
Clinical Research Associate I, PER DIEM - Tan Lab
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
A company is looking for a Clinical Research Associate to support multiple projects in the healthcare field. ...
Non-Clinical - Research Associate
REQUIRED EXP: Min yrs exp in a clinical research coordinator role with recent experience being in an Academic Medical Center. ...
Clinical Research Associate II - Division of Endocrinology, Diabetes, and Metabolism / Department of Medicine
As a Clinical Research Associate II, you will work directly with a Principal Investigator, Clinical Research Coordinator, Research Program Administrator, or Research Nurse to coordinate and/or implement the study and may serve as the point of contact for the external sponsors. The CRA II provides li...
Clinical Research Associate II
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. Sets up Study Master File and Study Master...
Senior Clinical Research Associate - Oncology - Los Angeles, CA
Primary interfaces: Provider Functional Manager, Clinical Trial Assistant, Local Trial Manager and Central Study Team for assigned clinical trials. As a Sr CRA you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. Develops si...
Clinical Research Associate
The Clinical Research Associate will provide support to the Senior Director, Clinical Operations in managing and tracking key study deliverables and milestones. Assist with the review and development of study-specific protocols, CRFs, clinical study plans, manuals, tools, trackers and templates, etc...
Senior Clinical Research Associate - Rare Disease / Respiratory - West Coast
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. ...