Clinical Research Data Associate I (Hybrid)

Details of the offer

Job DescriptionThe Clinical Research Associate I works directly with a Clinical Research Coordinator, Research Program Administrator, or Research Nurse to coordinate and/or implement the study. Evaluates and abstracts research data and ensures compliance with protocol and research objectives. Responsible for completing case report forms, entering clinical research data, and assist with regulatory submissions to the IRB. Provides limited patient contact as needed for study and assist with study budget and patient research billing. Ensures compliance with all federal, local, FDA, IRB, and HIPAA guidelines and regulations pertaining to the study and patient care.Primary Duties and ResponsibilitiesWorks with a Clinical Research Coordinator, Research Program Administrator or Research Nurse to coordinate/implement study.Evaluates and abstracts clinical research data from source documents.Ensures compliance with protocol and overall clinical research objectives.Completes Case Report Forms (CRFs).Enters clinical research data into Electronic Data Systems (EDCs) that are provided by the sponsors.Provides supervised patient contact or patient contact for long term follow-up patients only.Assists with regulatory submissions to the Institutional Review Board (IRB) including submission of Adverse Events, Serious Adverse Events, and Safety Letters in accordance with local and federal guidelines.Assists with clinical trial budgets.Assists with patient research billing.Schedules patients for research visits and research procedures.Responsible for sample preparation and shipping and maintenance of study supplies and kits.Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board.Maintains research practices using Good Clinical Practice (GCP) guidelines.Maintains strict patient confidentiality according to HIPAA regulations and applicable law.Participates in required training and education programs.QualificationsRequirements:High School Diploma/GED required. Bachelor's Degree preferred.Req ID : 3699Working Title : Clinical Research Data Associate I (Hybrid)Department : Cancer - SOCCI Clinical ResearchBusiness Entity : Cedars-Sinai Medical CenterJob Category : Academic / ResearchJob Specialty : Research Studies/ Clin TrialOvertime Status : NONEXEMPTPrimary Shift : DayShift Duration : 8 hourBase Pay : $23.00 - $29.87


Nominal Salary: To be agreed

Source: Whatjobs_Ppc

Job Function:

Requirements

Laboratory Associate I

We are searching for motivated, enthusiastic, and hands-on individuals interested in advancing science through the manufacturing of our CRISPR products. As a...


Menlo Ventures - California

Published 9 days ago

Senior Data Scientist

Come join the QB Live Analytics Team as a Senior Data Scientist. Our team works cross-functionally to improve and accelerate decision-making across the Exper...


Intuit Inc. - California

Published 9 days ago

Principal Research Scientist I

Company Description AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the med...


Allergan - California

Published 9 days ago

Research Scientist (Post-Training)

We are Genmo, a research lab dedicated to building open, state-of-the-art models for video generation towards unlocking the right brain of AGI. Join us in sh...


Genmo Inc. - California

Published 9 days ago

Built at: 2024-12-25T06:44:11.675Z