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Clinical Trials Oncologist. Provide compassionate clinical care and participate in research and clinical trials. Opportunity to partner with the Louisiana Cancer Prevention and Control Program (LCP), which is a series of programs, projects, and studies that currently covers breast, cervical, HPV, colorectal, lung, and other tobacco-related cancers.
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GxP, Life Science domain knowledge, Clinical Trials. Technologies: Oracle APEX, REST API s, PL SQL, Microsoft Azure, OCI, AWS, Node JS, JavaScript, CSS, HTML, JQUERY and AJAX. Familiarity with the healthcare or clinical research industry.
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Duration: 6 months Location: Foster City, CA (Hybrid) As a Clinical Trial Manager, you will: Job Description: FUNCTION: Clinical Operations - Biomarker and Bioanalytical Operations Clinical Operations is responsible for the worldwide execution of all Phase I - IV clinical trials across all client's therapeutic areas.
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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 Today - UpvoteDownvoteShare Job
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This is an exciting opportunity to learn about the biobanking and clinical trials process. The Associate will be a member of the Biorepository and Biomarker Core and be involved in clinical trials, translational research, and basic science research.
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As a part of Clinical Trials Scientific Affairs, the Principal Scientist will support testing, method development and validation. Collaborate with Research & Development, Scientific Affairs, and Laboratory staff in any way applicable to support Clinical Trials.
$115,000 - $130,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Job Req ID: 112971 Clinical Research Monitor The Department of Neurology is seeking a who will take the lead on compliance monitoring of predominantly large, multi-centered, clinical trials in keeping with established BIOS Clinical Trials Coordinating Center (CTCC) policies and procedures and GCP. The CRM will ensure quality, accuracy and integrity of clinical trial data throughout the full lifecycle of multiple clinical trials through utilization of a risk-based, remote monitoring approach.
$55,200 - $96,600 a year depends on experienceFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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ARA's Littleton office supports a variety of customers in electromechanical systems integration, wearable technologies development, edge processing and algorithms, and advanced sensor systems.
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Our investment is an early-stage BCI wearable tech startup employing an innovative mix of generative AI with recent breakthroughs in material science (patent-pending) for SOTA electronic consumer devices.
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Position Title: Patient Service Representative (PSR) Remote independent contract worker position Competitive fee for service Flexibility – work around your schedule Lifesaving medical technology The Cardiac Management Solutions division of ZOLL Medical Corporation develops products to protect and manage cardiac patients, including the LifeVest® wearable cardioverter defibrillator (WCD) and associated technologies.
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In accordance with provisions of approved protocols, the BPC serves as biorepositories for the Children’s Oncology Group (COG), NRG Oncology, SWOG (formerly the Southwest Oncology Group), the Pediatric Division of the Cooperative Human Tissue Network (pCHTN), Experimental Therapeutics Clinical Trials Network (ETCTN), and other sponsor groups.
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By unlocking the information present in microbial cell-free DNA, we're helping doctors quickly solve their most challenging cases, providing industry partners with access to the microbial landscape to accelerate biomarker discovery and clinical trials, discover novel microbes, to ultimately reduce patient suffering worldwide.
$206,469 - $309,703Full-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The Protocol Data Abstractor (PDA) Team Lead is responsible for managing the team of protocol data abstractors responsible for abstracting protocol content (e.g., lead organization, participating sites, study status information, IRB, funding) with new trials and amendments, performing data updates, addressing user inquiry requests, associated with clinical trials reporting.
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This role plays a pivotal role in coordinating and overseeing clinical operations of all assigned Clinical Research Nurse and Clinical Trials and participates in assessing, planning, implementing and evaluating Compliant Patient Care in clinical research studies.
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Educate patients and their families regarding clinical trials in general and the specifics of the proposed clinical trial. Coordinate patient care activities and conduct studies for patients enrolled in clinical trials.
$97,700 - $156,400ExpandApply NowActive JobUpdated Today
clinical trials wearable technologies jobs Title: opportunity
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