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The Staff Research Scientist will investigate, identify, develop, implement, and monitor systems to ensure that the assigned research projects/studies comply with Institutional Review Board (IRB) standards, scientific procedures, and stay within timelines for the Center for Autism Services, Science, and Innovation (CASSI, formerly known as the Center for Autism and Related Disorders, or CARD.
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The Research Assistant may also coordinate meetings with early intervention providers and Directors of Early Intervention programs in the Greater Boston area, assist with data collection from early intervention providers; review and score recorded intervention sessions for intervention fidelity and code recorded parent-child interactions for parent responsivity, manage and administer participant incentives, and manage Institutional Review Board (IRB) submissions.
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Contribute to the regulatory strategy, preparation, and review of regulatory submissions, response to IRB/EC questions, and participate in global health agency meetings. The ideal candidate is an MD or MD/PhD scientist with a clinical perspective, coupled with a track record of exceptional achievement in oncology therapy development.
ExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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Ensures regulatory integrity of protocols through the accurate and timely preparation and submission of documents and reports to the sponsor, IRB and other oversight bodies in accordance with federal regulations, sponsor SOPs and institutional policies.
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However, the applicant will also be responsible for literature reviews, study design, IRB submission, sample testing, medical record reviews, statistical analysis, and manuscript preparation. The clinical laboratory at BWH utilizes innovative technologies and dedicated staff to perform over 7 million tests per year for our patients at BWH and Dana Farber Cancer Institute, both affiliates of Harvard Medical School.
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Supports clinical trial readiness by working with clinical operations and CROs as needed for generation/review/editing of clinical study documentation including IRB/IBC communications/responses, study manuals, etc.
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Position Overview: The Institutional Review Board Manager will be responsible for the management of UMBC’s IRB program. The UMBC Research Compliance Program areas include Human Subjects Protections, Animal Care and Use, Institutional Biosafety Research, Export Control, Conflicts of Interest, Responsible Conduct of Research and supporting the Office of Research and Creative Achievement (ORCA) Vice President on requirements associated with allegations of misconduct in research and other scholarly activities.
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Tracks in a coordinated manner the IRB approval process, contract execution, ancillary approvals, credentialing requirements, regulatory documents, and other study-start-up requirements in partnership with the study PI and study team.
$66,700 - $103,400 a yearExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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The Clinical Research Coordinator is also responsible for keeping all data and source documentations, adverse event reporting, and IRB regulatory files. The primary responsibility of the Clinical Research Coordinator is to coordinate and conduct the day-to-day operation of clinical studies and clinical trials in cardiovascular and chronic kidney diseases.
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Administrative and Project Management: Obtain subject consent and assist with IRB and IACUC submissions or equivalent protocol, if applicable. Experience performing qPCR, qRT-PCR, DNA sequencing, ChIP-seq, mRNA isolation, northern blots, cDNA synthesis, immunoblots, co-immunoprecipitation, immunohistochemistry, and in situ hybridizations, are highly desired.
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The Clinical Research Coordinator A will recruit and screen patients as outlined in research protocols, will coordinate all research visit activities for assigned projects (including processing and shipping blood and urine samples), and will assist in the maintenance of research records in compliance with IRB and HIPAA regulations.
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Compiles JIT documents, IRB, IACUC, and Other Support pages while closely working with grants administrators. The Grant Coordinator works with Grant Administrators to develop and prepare grant applications and submissions, establish new research funds, provide monthly monitoring assistance of research funds, track budgetary performance, and submission of required reports for designated grants and contracts.
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Submit and manage IRB protocols related to asthma outcomes research. They will work under the supervision of the Division Director of Pediatric Pulmonary and Allergy, Dr. Robyn Cohen; the Physician Champion within Pediatric Primary Care, and in close collaboration with primary care Nursing and Operations leadership and BMC population health.
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Responsible for collecting, preparing and reviewing regulatory documentation for IRB submission prior to study start-up. Responsible for managing relationships with CROs and other vendors for all study activities including study start-up, close out, and completion of Trial Master File. Responsible for initial RFP obtainment and contributes to CRO/vendor selectionResponsible for setting up, negotiating, and monitoring Task Order invoice payments for CRO (direct service and pass through costs); as well as oversee scope change negotiations.
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Proficient knowledge of IPv4 and IPv6 Networking, Routing (OSPF/BGP/ISIS/PIM) and Switching (STP/SVI/VLAN, IRB/BVI) Cisco Certified (CCNP, CCIE) - Industry and vendor specific certifications and training preferred (Cisco, Juniper, Nokia, etc.
$124,000 - $220,000Full-timeExpandApply NowActive JobUpdated 2 days ago
irb job
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