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Uniquely focused on community-based Hematology & Oncology research sites, we provide real-world experience, data, and outcomes that lead to improved clinical utility of cancer therapies, improving the lives of cancer patients.
$65,000 a yearExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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The Clinical Research Quality & Regulatory Specialist plays an integral role in the data integrity and regulatory compliance of pharmacy services related clinical research.
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Manage Clinical Data Specialists to ensure all aspects of study data collection, management, and analysis meet the requirements to support regulatory submission of bioMérieux's molecular in vitro diagnostic products or other research activities.
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TheEmmesCompany, LLC(“Emmes”) isa global, full-service Clinical Research Organization dedicated to excellence in supporting the advancement of public health and biopharmaceutical innovation.
ExpandApply NowActive JobUpdated 9 days ago - UpvoteDownvoteShare Job
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SAS, Programmer, statistics, CDISC, SDTM, ADaM, CRO, clinical research, pharmaceutical, biotechnology, clinical data, data management, EDC, Electronic Data Capture, Medidata, Rave, Oracle, Inform, datasets, TLF, tables, listings, figures, programming, benefits, medical, dental, vision, 401k, Remote.
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Trains and develops staff to ensure operational objectives for ST conform to all relevant federal and state laws, regulations, guidelines; clinical research protocols, internal SOPs and WIs.
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Clinic Research Coordinator II The Clinical Research Coordinator II , will ensure that quality research is conducted at the assigned investigative sites in accordance with the sponsor protocol, FDA Regulations, and ICH/GCP guidelines and to provide the best quality data to the sponsor.
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Data Entry and Verification: Assist with the transcription and data entry of Source Documents and Case Report Forms (CRFs) into research management systems, maintaining data integrity and responding to queries in Electronic Data Capture (EDC) systems.
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Conduct monitoring visits and activities in accordance with FDA Code of Federal Regulations, GCP guidelines, departmental SOPs, Work Instructions and the Clinical Monitoring Plan. Use of EDC and other electronic tools to review monitor listings and queries.
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Clinical Research Coordinator; experience as a CRC & bilingual/fluent in Spanish is REQUIRED. The candidate will be coordinating clinical research protocols from study start up to close out.
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This position will start as a Sub-Investigator but will blossom eventually into a Clinical Research Principal Investigator. Great opportunity to get into clinical research for the first time or continue a career with an organization 100% focused on bettering the clinical trial process.
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Work Performed: (Position Specific and Non-Specific Tasks) Perform a variety of research, data base and clerical duties of a complex and technical nature in support of multi-center clinical trials to assist investigators in organizing, gathering and compiling clinical research data.
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Basic understanding of clinical research (pharma, device and/or biotech sectors) and of Clinical Research SaaS technology. Self-motivated and able to assume responsibility in a professional mannerIs proficient in the use of all relevant EDC/CDM systems.
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Piper Companies is looking for an experienced Senior Statistical Programmer (PK/PD) to join a well-established, global clinical research organization focused on improving the drug development process and access to therapeutics.
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With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners' most high-profile drug and device programs.
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