1 day ago Be among the first 25 applicants CEDARS-SINAI has partnered with iHire to reach top talent for their opening below. Check it out and apply via iHireBiotechnology today! Primary Duties And 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. 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. Works 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. Qualifications Requirements High School Diploma/GED required. Bachelor's Degree preferred. Req ID: 4666 Working Title: Clinical Research Associate I, PER DIEM - Tan Lab Department: Cancer - Research Center Health Equity Business Entity: Cedars-Sinai Medical Center Job Category: Academic / Research Job Specialty: Research Studies/ Clin Trial Overtime Status: NONEXEMPT Primary Shift: Day Shift Duration: 8 hour Base Pay: $19.50 - $32.86 Seniority level Entry level Employment type Part-time Job function Science, Research, and Engineering #J-18808-Ljbffr iHire
...information is subject to a number of factors including but not limited to experience and education.For additional information on this opportunity, contact Karen Smith directly at (***) ***-****. Resumes may be confidentially sent to ****@*****.***.#J-18808-Ljbffr gpac
...Requirements ~ BSN Degree Overview Memorial Hospital Belleville is an acute care hospital offering medical and surgical... ...Education ~ Nursing Diploma/Associate's - Nursing Experience ~2-5 years Supervisor Experience ~ No Experience...
...Because whatever your background, skill set or career goals, you'll find there's always room at our table. PRIMARY PURPOSE Our florist clerks are a bunch of experts. They arrange beautiful displays for our customers, stock shelves, maintain displays and make sure...
...of partnership to protect peoples health; to preserve magnificent places and wildlife; to advance clean energy; and to combat climate change. We partner with thousands of groups, supporters, individuals and communities to engage the critical environmental issues of our...
...Project Manager II # 25-103 Job Title: Project Manager II Location: Chicago, IL 6... ...role Job Profile Summary The Business Transformation Project Management contractor... .... Qualifications: ~ Bachelors degree or equivalent work experience ~5+ years...