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The Synthetic Biology Applications Development Manager serves as a key liaison to the scientific community, demonstrating how our synthetic biology solutions work and developing relationships with key opinion leaders and stakeholders, through collaborations and publications to gain IDT broader market access and awareness.
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We’re investing €400m a year into the new Center, hiring a team of 400 dedicated employees for it and using it as the foundation to implement integrated end-to-end mRNA vaccine capabilities and research with R&D, digital and CMC teams.
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Liaise with Clinical Sample Management for the tracking and coordination of biomarker testing with 3rd party labs. In over 10 years since its inception, Moderna has transformed from a research-stage company advancing programs in the field of messenger RNA (mRNA), to an enterprise with a diverse clinical portfolio of vaccines and therapeutics across seven modalities, a broad intellectual property portfolio in areas including mRNA and lipid nanoparticle formulation, and an integrated manufacturing plant that allows for rapid clinical and commercial production at scale.
$56,000 - $89,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Conducts Pre-Registration tasks for specified inpatients and outpatients prior to their date of service including: collects demographic, financial, and clinical information necessary for financial clearance of scheduled patients; obtains missing insurance information via patient’s family or physician offices; and completes insurance verification using online electronic verification system or contacting payor directly.
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Ensure provision of appropriate, timely, and effective addiction recovery treatment for patients on a Level IV Detox Unit. Employs a range of clinical interventions such as individual, group, and family treatment.
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The Senior Clinical Database Programmer (RAVE)is responsible for developing EDC database, contributing to the assessment and tracking of quality of programming tasks and activities executed by CRO and FSP vendors performing clinical trial programming work for Biogen.
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New Solutions: Provides technical expertise, application support, training, guidance, and written proposals that may include application products from Vendors such as Veritas, Commvault , EMC, IBM, Innovation Data Processing, Rocket, and other applications designed for data protection.
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Provide support for NetSuite, Salesforce, and Procore applications, providing advanced troubleshooting and resolution of complex issues. Manage user accounts, permissions, and settings for Microsoft 365, Salesforce, NetSuite, Procore and other cloud-based applications according to documented procedures.
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The Senior Sales, Genetic Testing Specialist (GTS representative) will concentrate on growing the company's genetic testing business across areas such as Pharmacogenomics, infectious disease, and oncology.
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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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As a Visual Information Specialist, you will be creating visual information materials, including digital and print graphics, video, audio, and multimedia programs. design, applications, layout, make-up, and production; utilizing Adobe Creative Cloud applications, including Premiere, After Effects, Photoshop, Illustrator, and InDesign; peripheral computer equipment; operating various audiovisual equipment; and equipment and Public.
$59,966 - $140,713 a yearFull-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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With a combination-focused pipeline that exploits the power of six scientific platforms (Immuno-Oncology, Tumor Drivers and Resistance, DNA Damage Response, Antibody-drug Conjugates, Cell Therapy and Epigenetics) to help address unmet clinical needs in a host of hematological cancers, we are motivated by a dedication to the scientific discovery and collaboration that will one day help eliminate cancer as a cause of death.
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Highly competent in clinical data management, various EDC systems, CDR systems, CDASH/CDISC standards, and medical coding dictionaries. Act as CDM subject matter expert, drive Transformation Initiatives in partnership with the business and leverage technical and functional expertise across Clinical development operations, Clinical development, DDI, Safety, GBS, etc.
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Previous experience as a clinical research coordinator, regulatory associate, and/or start-up specialist is valuable. The Senior Clinical Regulatory Specialist will work under the direction of the Clinical Regulatory Manager with the primary responsibility of assisting with the conduct and compliance of Phase 2-4 pharma sponsored research studies.
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In this position, you will serve as an Emergency Management Specialist (Mitigation) in the Region One, Mitigation Division of the Hazard Mitigation Assistance Branch. In this position, you will serve as an Emergency Management Specialist (Mitigation) in the Region One, Mitigation Division of the Hazard Mitigation Assistance Branch.
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Title: clinical applications specialist in Belmont, MA
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