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Senior Clinical Research Coordinator
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Research Coordinator
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Research Coordinator
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Research Coordinator
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Research Coordinator
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Research Coordinator
1 day ago
University of California Los Angeles, United StatesUnder the supervision of the Clinical Research Center Administrator, provide coordination support for Department of Ophthalmology Clinical Research Center. Clinical Research Center duties include coordinating the daily aspects of clinical trials and other clinical studies, as ass ...
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Clinical Research Coordinator
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Clinical Research Coordinator
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Clinical Research Coordinator
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LanceSoft, Inc. Los Angeles, United StatesTitle: Clinical Research Coordinator · Location: Los Angeles, CA 90025 · Contract duration: 13 weeks · Shift: 08:00am - 17:00pm · Expected Hour's: 40hrs/wk. · ***TEMP TO PERM*** · ***LOCALS PREFERRED*** · Summary/Duties: · Screening and recruitment of potential patients for proto ...
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Clinical Research Coordinator
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Clinical Research Coordinator
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Clinical Research Coordinator
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Medix™ Glendale, United StatesThe Clinical Research Coordinator works independently providing study coordination including screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. Responsible for accurate an ...
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Clinical Research Coordinator
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Medix™ Glendale, United StatesClinical Research Coordinator - Glendale, CA · Location: Glendale, CA · Schedule: Monday-Friday · Pay: $62,000 - $85,000 · The Clinical Research Coordinator works independently providing study coordination including screening of potential patients for protocol eligibility, prese ...
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Research Coordinator
2 weeks ago
The Lundquist Institute Torrance, United States**Required Skills & Qualifications**: · - BS degree in Biology, biomedical science, biomedical engineering. · - Ability to establish and maintain effective working relationships with all levels of campus and hospital · administration staff, faculty and industry sponsors · - Abili ...
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Clinical Research Coordinator
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Headlands Research Palos Verdes Peninsula, California, United States PermanentOverview: · Headlands Research and Peninsula Research Associates are working together to build the best clinical trial company in the world. We're an exceptional family of next-generation clinical trial sites, integrating cutting edge technology and high-quality support services, ...
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Clinical Research Coordinator
1 week ago
PIH Health Whittier, United States Full timeThe Clinical Research Assistant (CRC) works collaboratively with Principal Investigators (PI) sub-investigators, clinical and ancillary departments, to assist with research studies in subject recruitment, data collection, scheduling of study-related activities, and follow-up of e ...
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Clinical Research Coordinator II
3 weeks ago
Cedars-Sinai Beverly Hills, United StatesThe Clinical Research Coordinator II serves as the lead coordinator on an assigned portfolio of research studies, functioning independently to establish and coordinate logistics and processes for the conduct of research for the department. This individual will interact with princ ...
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Research Coordinator II
8 hours ago
University of Southern California Los Angeles, United StatesUSC's Keck School of Medicine, Medicine Research Unit within the Department of Medicine is seeking a Research Coordinator II to join its team. The Research Coordinator is responsible for coordinating assigned projects. The Research Coordinator II po Research Coordinator, Research ...
Clinical Research Coordinator I - El Segundo, United States - Cedars-Sinai
![Cedars-Sinai background](https://contents.bebee.com/companies/us/cedarssinai/background-9Dx57.png)
Description
Job Description Come join our teamThe Clinical Research Coordinator I works independently providing study coordination, screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process.
Responsible for accurate and timely source documents, data collection, documentation, entry, and reporting including timely response to sponsor queries.Responsible for compiling and reporting on each study including information related to protocol activity, accrual data, workload, and other research information.
Presents study information at regular research staff meetings.Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board (IRB).
Primary duties and responsibilities:
Independent study coordination including screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details to the patients, and participating in the informed consent process.
In collaboration with the physician and other medical personnel, documents thoroughly on Case Report Forms (CRFs) the following; changes in patient condition, adverse events, concomitant medication use, protocol compliance, response to study drug.
Maintains accurate source documents related to all research procedures.Responsible for accurate and timely data collection, documentation, entry, and reporting including timely response to sponsor queries.
Schedules and participates in monitoring and auditing activities.
Responsible for compiling and reporting on each study including information related to protocol activity, accrual data, workload, and other research information.
; present this information at regular research staff meetings.Notifies direct supervisor about concerns regarding data quality and study conduct.
Works closely with a regulatory coordinator or directly with the Institutional Review Board (IRB) to submit Adverse Events, Serious Adverse Events, protocol deviations, and Safety Letters in accordance with local and federal guidelines.
May perform other regulatory / Institutional Review Board duties, budgeting duties, and assisting with patient research billing and reconciliation.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 Educational Requirements:
High School Diploma/GED required
Bachelor's Degree in Science, Sociology or related degree preferred
Licenses:
SOCRA or ACRP Certification preferred upon hire
Experience:
One (1) year of clinical research related experience required
About Us Cedars-Sinai is a leader in providing high-quality healthcare encompassing primary care, specialized medicine and research.
Since 1902, Cedars-Sinai has evolved to meet the needs of one of the most diverse regions in the nation, setting standards in quality and innovative patient care, research, teaching and community service.
Today, Cedars- Sinai is known for its national leadership in transforming healthcare for the benefit of patients. Cedars-Sinai impacts the future of healthcare by developing new approaches to treatment and educating tomorrow's health professionals. Additionally, Cedars-Sinai demonstrates a commitment to the community through programs that improve the health of its most vulnerable residents.About the Team Cedars-Sinai is one of the largest nonprofit academic medical centers in the U.S., with 886 licensed beds, 2,100 physicians, 2,800 nurses and thousands of other healthcare professionals and staff.
Choose this if you want to work in a fast-paced environment that offers the highest level of care to people in the Los Angeles that need our care the most.
ReqID :
1131
Working Title :
Clinical Research Coordinator I - Obstetrics & Gynecology - Accortt Lab (Full-Time)
Department :
Research - OBGYN
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 :
$ $39.76
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