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SUPERVISORY RESPONSIBILITY (if applicable): A Clinical Research Coordinator I does not have any supervisory responsibility. A Clinical Research Coordinator II may assist with the training and orientation of new staff members.
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Job Overview: The Senior Research Associate will conduct scientific work on innovative therapies, analyze data, and collaborate with team members in a fast-paced environment. BS/MS degree in a biological science or equivalent, with at least 3-5 years of research experience in immunology, preferably in an industry setting.
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We are looking for a highly motivated research associate with the ability to work both independently and collaboratively. Innovate and expand our assay portfolio by identifying, evaluating, and implementing new assay technologies through literature research, academic collaborations, and adaptation from other groups within the company.
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The Sethi Laboratory at the Dana-Farber Cancer Institute and Harvard Medical School is seeking a highly motivated, creative, collegial and dedicated full-time research technician with a bachelor's in biology or related field to join their group.
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Strong knowledge of biomarker technologies and methodologies, including genomics, proteomics, imaging, and flow cytometry, as applied to clinical research. Ph. D. or equivalent degree in Molecular Biology, Biochemistry, Pharmacology, or related field with a minimum of 8 years of relevant experience in clinical biomarker research within the biopharmaceutical industry.
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Our interdisciplinary scientists steward a breadth of efforts that encompass research on plants to groundwater science and coastal zones, to storm prediction. At PNNL, you will find an exciting research environment and excellent benefits including health insurance, flexible work schedules and telework options.
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JOB SUMMARYThe Research RN, NCHRI works directly with the physician in accurately and professionally executing all clinical research projects in an acute care/inpatient setting (ED, Cath Lab, ICU, EP lab, Step down and OR) as well as the ambulatory and ancillary areas.
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The Consultant Pharmacist IV will assist in the development and management of the MassHealth Drug List, clinical initiatives, Accountable Care Organization pharmacy oversight and other pharmacy programs.
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Research, clinical operations, clinical pharmacology, translational medicine, biostatistics, regulatory, safety, CMC, commercial operations. Experience providing scientific support for the development and implementation of cell therapy studies, including protocol and ICF development, electronic data capture database development, safety assessment, IB/DSUR submissions, and clinical data review.
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Creates a documentation system chronicling all incoming/outgoing clinical documentation, maintains study supply documentation, reviews Study Folder regularly to ensure file accuracy and completeness, maintains study specific metric tracking and reviews Clinical Research Associate (CRA) field monitor reports and any necessary follow-up letters in relation to specific Study Monitoring Plan, contacting CROs and CRAs, as required.
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Strong knowledge of drug discovery and development processes, including preclinical and clinical research. The Research Strategy and Operations function is responsible for integrating scientific acumen with business analytics and processes to deliver clear business plans, operational excellence and portfolio progression for the Takeda Research pipeline.
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Manages all aspects of protocol implementation between the multi-site research team at BWH and collaborators at University of Maryland, Baltimore (UMB), Harvard Hebrew Senior Life, PointClickCare (SNF EHR vendor), ZCO (patient app development vendor), and the 32 clinical research sites.
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Our client, a leader in the pharmaceutical industry, is seeking a Research Associate, Analytical Development to join their team. Perform UV, HPLC, SV-AUC and CE-based methods to quantitatively measure the purity of the AAV gene therapy vectors and support process development.
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Oversee the planning, implementation, and management of immuno-oncology clinical trials from initiation to completion. The Senior Clinical Trial Manager will play a crucial role in overseeing and managing Phase 1-3 clinical trials related pertaining to mRNA therapies targeting cancer and rare disease.
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Additionally, the Community Awareness Associate facilitates external community and provider workshops and supports the Capacity Building Manager with our annual Screening Tool Conference, which teaches providers in MA how to distinguish between the abuser and the survivor in LGBTQ+ relationships where partner abuse is happening.
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Title: clinical research associate Company: Global Strategic Solutions Division Of Icon Plc in Boston, MA
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