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As a Clinical Research Analyst, you'll be at the forefront of cutting-edge research, playing a pivotal role in managing protocols within the Clinical Trials Management System (CTMS), OnCore, for both the Academic Health Center (AHC) and Oncology (ONC) human subject clinical research projects under CRH's purview.
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Experience working in a Clinical setting(i.e.,nurse, research coordinator, research manager) The field based clinical professionalrolefocuses on engagement with institution-basedhealthcare providersworking on clinical trials (i.e.,Principal Investigators, Sub Investigators, Research Managers,and Clinical Research Coordinators.
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1-3 years of experience in a relevant field supporting clinical trials through a clinical site, CRO or trial sponsor, clinical research coordinator Ability to travel 25%-50% of the time during peak periods Understanding and application of GCP, ICH, and applicable regulatory standards governing clinical research Excellent written and oral communication and presentation skills The ability to manage multiple priorities, while maintaining attention to detail is critical.
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Clinic Research Coordinator II The Clinical Research Coordinator II , will ensure that quality research is conducted at the assigned investigative sites in accordance with the sponsor protocol, FDA Regulations, and ICH/GCP guidelines and to provide the best quality data to the sponsor.
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The RA II will be the main clinical trial liaison for the investigative research team, the research subjects, and the Sponsor. This highly motivated individual will have excellent interpersonal skills and the ability to multitask, conduct technical and administrative aspects of the research study including: coordination of staff and participants; lead study recruitment activities, coordinate study assessments and intervention activities, safety reporting, management of data and study documentation for Institutional Review Board (IRB), clinical research forms, and quality assurance.
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IQVIA is seeking Senior Clinical Research Associate IIs and Senior Clinical Research Associate IIIs based in the Mid-West, US and Northwest, US. Ideal candidates will have at least 4+ years of on-site monitoring experience.
$111,972 - $174,468 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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A Site Manager I (SM I) serves as the primary contact point between the Sponsor and the Investigational Site. A SM I is assigned to trial sites to ensure inspection readiness through compliance with the clinical trial protocol, company Standard Operating Procedures (SOP), Good Clinical Practice (GCP), and applicable regulations and guidelines from study start-up through to site closure.
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Communicate effectively with subjects, research team, Institutional Review Board (IRB) and sponsor representatives. Clinical skills that may be required include, but not limited to: patient assessment for adverse events and assistance with, or completion of, study related procedures as detailed in the research protocol (ex: injections, phlebotomy, or infusions), within the applicable state scope of practice.
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2 years of clinical research coordinator experience strongly preferred. IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry.
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The site director will also ensure that quality research is conducted at assigned investigative sites in accordance with the sponsor protocol, FDA Regulations and ICH/GCP guidelines and to provide the best quality data to the sponsor.
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0-1 year experience in a medical setting and/or clinical research preferred. Attends clinical research-related training as required. Under close supervision, ensures documents and forms are compiled and submitted in a timely manner to the CRO, study sponsor or IRB as applicable.
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Support all aspects of clinical research data management for clinical trials conducted in the LCCC Clinical Research Management Office (CRMO), including collection of data from source documents and medical records and completion of case report forms per sponsor requirements.
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Minimum two years ObGyn clinical research experience preferred; epidemiology background helpful. Our extraordinary professionals are continuously discovering clinical innovations and enhanced access to the most up-to-date facilities, equipment, technologies and research protocols.
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Will serve as a liaison between the Center Business Office, Principal Investigators (PIs), fiscal and administrative support personnel, clinical research staff, and central Research Support Services divisions, and develop strategies to optimize and grant and contract management process.
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CRC (Clinical Research Coordinator) Certification preferred (ACRP) 5.1 Responsible for processing of contract in conjunction with Bridgeport Hospital legal counsel, Sponsor, and Principal Investigator.
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