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Our office promotes and facilitates clinical research by providing comprehensive services to physicians conducting clinical trials while ensuring compliance with all regulatory requirements.
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The Clinical Research Coordinator assists the clinical trials process by registering hematology, oncology, and bone marrow transplant patients for clinical studies, assessing eligibility criteria, maintaining current protocol packets and assuring that all quality assurance measures are maintained within the protocol/study.
$39,300 - $64,349 a yearFull-timeExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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Demonstrated knowledge of all components of the research process as it pertains to clinical trials and studies, i.e., IRB procedures and processes, data management, etc. Study Coordinator, Clinical Research Coordinator, Clinical Research Regulatory.
$30 - $35 an hourExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Uses clinical research management system and its reports to manage all protocol activities, including minimum footprint, SIP counsel, and all aspects of maintaining current protocol information.
$60,608 - $66,458 a yearFull-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Experience in clinical research, familiarity with oncology protocols, clinical trials operations, GCP, NCI guidelines and federal regulations both FDA and HHS. Experience 2-5 Years' experience as a Clinical Research Associate, Clinical Research Coordinator, Clinical Research Nurse Coordinator and proven experience as an Lead Auditor.
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You will work in a supportive Research and Development team, and collaborate cross-functionally including the clinical team, manufacturing team, and other various functions. Design and manage translational studies for clinical trials including PK/PD, safety or biomarker analysis.
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This is an exciting opportunity for clinical research professionals with at least one year of Clinical Research Coordinator experience to fill Clinical Research Associate (CRA) openings with Medpace.
$50,000 - $100,000 a yearExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Through research, teaching, service, and outreach, UConn embraces diversity and cultivates leadership, integrity, and engaged citizenship in its students, faculty, staff, and alumni. UConn is a Carnegie Foundation R1 (highest research activity) institution, among the top 25 public universities in the nation.
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Our Plano campus is looking for an experienced Clinical Research Coordinator who will play an important part in coordinating drug treatment research trials within the Hematology and Oncology teams, as well as observational studies.
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The person will support Infectious Disease Physician Investigators in clinical research ranging from observational trials to investigational drug/product trials, including investigator-initiated, government funded, and industry-sponsored trials.
$42,953 - $77,315 a yearExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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As the Manager, Clinical Data Management you will be responsible for data management in clinical trials across all therapeutic areas. Responsible for all clinical data management activities in clinical trials in accordance with Ferring SOPs and current regulatory requirements.
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Knowledge of clinical research process inclusive of Phase I trials through regulatory submission. To drive continued success in this exciting clinical research field, we are seeking committed, skilled, and customer-focused individuals to join our winning team as a Senior Project Manager for our Bridgewater, New Jersey, USA on-site location, or remotely from a home-based office anywhere in the USA in accordance with our Work from Home policy.
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The fellow will have the opportunity to participate in a range of clinical research studies, including randomized clinical trials on weight loss, time restricted eating, remotely delivered adaptive interventions, and projects that are developing and validating methods to quantify food intake and related behaviors with smartphone apps.
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The Clinical Research Nurse Manager supervises compliance and educational activities within the Institution as it relates to clinical trials and preclinical studies. 0) Shift: Shift 1 Work Schedule: 8 Hr (8:00:00 AM - 5:00:00 PM) Summary: The Clinical Research Nurse Manager is a professional registered nurse who is responsible for the oversight of all clinical and preclinical research activities, including clinical care for patients enrolled in trials at Rush University.
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St. Jude Children's Research Hospital offers a unique environment with clinical and basic science investigators working in close proximity and interacting regularly to translate scientific discoveries into improved therapies for children.
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clinical research jobs Title: clinical trials Company: Parexel
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