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Lead, implement and coordinate duties for assigned clinical trials including but not limited to study start up, vendor management, subject recruitment, source document review and completion, protocol training, collection of regulatory documents, participant visits, timely data collection and documentation, management and reporting of adverse events, serious adverse events, and deviations, and monitoring visits and follow up.
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The Clinical Research Coordinator handles or assists with the administrative activities generally associated with the conduct of clinical trials and mixed methods research specific to LGBTQ+ populations.
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Successful completion of GCP certification and Certified Clinical Research Coordinator (CCRC) certification within 6 months of being in the role. The Clinical Research Coordinator will manage all clinical trial activities under supervision in compliance with all applicable laws, regulations, and procedures of study protocol while maintaining company mission, vision and values.
Full-timeExpandApply NowActive JobUpdated 14 days ago - UpvoteDownvoteShare Job
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Responsibilities: Conducting all trial visits Completing all study-specific assessments (e.g. vital signs, EKG, blood collection) Processing all samples and shipping to Central Lab Maintaining study source Entering data into sponsor EDC and query resolution as the sole Senior Clinical Research Coordinator (SCRC) on-site, the chosen candidate must be adept at protocol comprehension and be capable of working autonomously.
$56 an hourExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Description Clinical Research Coordinator B ResponsibilitiesThis individual will work under general supervisionThe CRC will be responsible for the coordination of complex oncology clinical research protocols, including accurate data collection and overseeing the quality of the clinical trial data and records, scheduling and conducting study initiation and monitoring visits, and participating in ongoing study protocol training.
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Demonstrated ability to work independently, make informed decisions, and drive clinical trials forward Track record of managing multiple clinical trials simultaneously with meticulous attention to detail Strong prioritization skills, adept at meeting deadlines, and flexible in adapting to shifting priorities Proficiency in phlebotomy (certification not mandatory.
$58 an hourExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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We are seeking a clinical research coordinator to assist with several ongoing clinical trials within this grant. JOB DESCRIPTION AND POSITION REQUIREMENTS:The Penn State College of Medicine, Department of Public Health Sciences, in Hershey, PA is seeking a Clinical Research Coordinator.
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We are looking for a dedicated Clinical Research Coordinator with phlebotomy experience to manage and oversee clinical trials. This position requires excellent organizational skills, strong attention to detail, and experience in clinical research and phlebotomy.
$40 an hourFull-timeExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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5+ years of experience coordinating Clinical Research trials. Job Title: Senior Clinical Research Coordinator. Clinical Research Coordinator.
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Reporting directly to Clinical Research Supervisor II, responsible for coordinating and managing clinical trials including providing all aspects of protocol management, including screening for patient eligibility, data collection and analysis, ensuring protocol compliance, adverse drug reaction reports, monitoring patient treatment and toxicities, laboratory and specimen submission, and maintenance of accurate and complete clinical research files.
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Title: Clinical Research Coordinator Location: Rochester Hills, MI Schedule: 8a-5p Type: Contract, 6 months Start Date: ASAP Joule is currently looking to hire a Clinical Research Coordinators at a Rochester Hills, MI site.
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We focus on sample collection and testing trials for lab device manufacturers with the purpose of collecting data to support the device's 510(k) or emergency use approval by the FDA. Notably, the trials we have participated in have directly led to the FDA EUA approval of three separate COVID-19 PCR testing platforms.
$25 an hourFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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We are looking for a Clinical Research Coordinator to help manage and oversee clinical trials and research studies. Data Collection: Collect and record data accurately from participants during the study.
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This role involves managing clinical research studies in compliance with operating procedures, ensuring the integrity and quality of clinical trial data through accurate data collection and reporting.
$40 - $45 an hourExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Advanced nursing position that involves clinical patient contact, research study coordination and study data management. Must be able to organize complex components of clinical trials, including test ordering, procedure scheduling and insurance pre-authorization for participants, if applicable.
$41.5 an hourFull-timeExpandApply NowActive JobUpdated Today
clinical research data collection trials jobs Title: clinical research coordinator
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