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Processing order requests for non-revenue generating inquiries: sample orders, swatch requests, Design Trunks, photoshoots, hospitality donations, etc. This includes general queries, sample orders, swatch requests, Design Trunk purchases, photoshoot and hospitality collaborations, and more.
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Embark on your career journey as a Sample Coordinator where you can develop and advance within our growing team! We have openings for a Sample Coordinator to join our team.
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Manages sample processing, packing, and shipping according to protocol, applicable standards, and regulations. We are looking for a dedicated clinical research professional to join our dynamic team as a Clinical Research Coordinator.
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Service coordinator back up for phones, quoting, and parts shipping. We specialize in the development, manufacturing and customization of precision measurement devices, automated liquid handling stations, and sample management systems.
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Communicates via phone and email with our IVF clinic partners regarding courier requests for patient samples, sample kits, and/or shipping supplies. The Logistics Coordinator (temporary) coordinates and arranges inbound shipments of patient samples from IVF clinic partners from around the world to our various CooperGenomics laboratories.
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Input, maintain & understand all biospecimen-relevant information in CLBM/BioMarin systems for clinical trial studies, including: outlining biospecimen stakeholder contacts, number and quantity of each biospecimen collected as related to the studys schedule of events, any unique biospecimen handling or operational requirements, details of testing destinations and related shipping requirements.
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Plans and performs research specimen collection, labeling and storage/shipping if assigned; maintains accurate sample accountability/chain of custody documentation. The Clinical Research Coordinator participates in or leads day-to-day operations of clinical research studies conducted by a principal investigator.
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Perform interdisciplinary activities coordinating new item set-up with Operations, Sales, Food Safety & Product Quality, Accounting, Maintenance, and Shipping/Receiving. Sample Coordinators play a crucial role, ensuring our customer's products meet the highest standards from ideation to production.
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Schedules and performs patient procedures, assessments, evaluations and testing as required by the protocol, including but not limited to blood sample collection, processing and shipping, ECG, vital signs, etc., as applicable.
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We are looking for a self-starter to join our team as a Clinical Research Coordinator. We are looking for a self-starter to join our team as a Clinical Research Coordinator. We are looking for CRC's with over 2 years of experience in clinical research.
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The Senior Clinical Research Coordinator will develop a progressive functional knowledge of Good Clinical Practices (GCP), Office of Human Research Protections (OHRP) regulations and Food and Drug Administration (FDA) regulations.
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Overview: We are looking for a qualified and experienced Research Coordinator. Our multi-disciplinary team approach includes surgical oncology, medical oncology, radiation oncology, women's centers, diagnostic imaging services, integrative services including social work and nutrition, and genetic counseling.
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The Cancer Center Protocol Office is seeking a motivated, detail-oriented individual to join our team as a Clinical Research Associate/Clinical Research Coordinator within the Pediatric Oncology Clinical Research Group at MGH. The Cancer Center Protocol Office is a centralized research office that supports clinical researchers in all disciplines within the Cancer Center.
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The Clinical Research Associate/Clinical Research Coordinator I (CRA/CRC I) works under general supervision to enroll eligible patients to clinical research protocols and manage all aspects of data collection and submission for multiple cancer studies.
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The Sylvester Comprehensive Cancer Center has a great opportunity for a Clinical Research Coordinator 3. The Clinical Research Coordinator 3 serves as an experienced clinical research professional responsible for providing leadership in the planning, implementing, monitoring, and evaluating of multiple clinical research protocols.
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