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The Research Associate Clinical I-Data Manager will help the study team in preparing for monitoring visits and audits and ensure compliance with all federal and local agencies including the Food and Drug Administration ( FDA ) and local Institutional Review Board ( IRB.
$17.24 - $27.59 an hourFull-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Under the supervision of ADRC principal investigator (Dr. Victor Henderson) and clinical research manager (Veronica Ramirez), main duties include in-person and telephone recruitment of research participants; obtaining informed consent; scheduling and coordination of research participant visits; maintaining longitudinal contact with participants by phone, email and other means; data collection (particularly including psychometric data), scoring, and entry.
$31.73 - $36.54 an hourExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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Collect and manage patient and laboratory data for clinical research projects. The Stanford ADRC seeks a full-time Clinical Research Coordinator Associate. Clinical Research Coordinator for Cognitive Aging Studies.
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The Clinical Research Associate II-RN is responsible for performing data abstraction, collection, and entry to support clinical research. Perform data abstraction, collection, and entry to support clinical research.
$70,720 - $126,880 a yearFull-timeExpandApply NowActive JobUpdated 23 days ago - UpvoteDownvoteShare Job
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Build data files and manage data entry of all data, maintain an updated and organized literature library, and ongoing communication with the research team(s) to maximize study objectives as well as the collection of data at required study points per study protocol(s)+ Provide regulatory compliance support to include preparation of IRB amendments, annual report, etc.
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Understanding of clinical research activities including tasks associated with study start-up, interim monitoring, closeout, data collection, and central files. Support and/or lead clinical research study start-up activities (including creation of study binders, study logs, work instructions, case report forms, and other study-related materials.
ExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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Ability to train site personnel on study activities including investigational product usage, maintenance and accountability, sample collection, testing and shipping, data entry, and query resolution.
ExpandApply NowActive JobUpdated 9 days ago - UpvoteDownvoteShare Job
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Clinical Research Associate (CRA) - B. Support and/or lead clinical research study start up activities (includes creation of study binders, study logs, work instructions, case report form, and other study related materials.
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Basic knowledge of, and skill in applying, applicable clinical research regulatory requirements (i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
Full-timeExpandApply NowActive JobUpdated 18 days ago - UpvoteDownvoteShare Job
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IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.
$73,780 - $110,670 a yearFull-timeExpandApply NowActive JobUpdated 18 days ago - UpvoteDownvoteShare Job
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Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
$73,780 - $110,670 a yearFull-timeExpandApply NowActive JobUpdated 18 days ago - UpvoteDownvoteShare Job
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This will include data entry in excel and / or JMP, consumer use test product preparation, team paneling, logistics (e. Job Description: I currently have an immediate need for a senior research associate to enable product modeling and execute consumer test product evaluations, placement logistics, and analysis.
ExpandApply NowActive JobUpdated 24 days ago - UpvoteDownvoteShare Job
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Job Title: Clinical Research Associate. Not Remote or Hybrid Our focus is on local candidates who want to work 100% in person and have 2-5 years previous clinical research experience.
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Clinical Research Associate. Support or lead clinical research study start up activities (includes creation of study binders, study logs, work instructions, case report form, and other study related materials.
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2-5 years' work experience with data entry, and clinical research industry, preferably within the ophthalmology field. 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.
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clinical research data entry jobs Title: clinical research associate
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