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The Clinical Research Coordinator II conducts and manages multiple clinical trials from start up through study close out in accordance with the study protocol, GCP, and Velocitys SOPs.
ExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Completes and oversees analysis of protocol documents to generate study database design specifications including CRF/eCRF design, visit schedule, edit checks, system notifications, query logic, user role setup, randomization triggers, supply triggers, and medical coding.
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Serves as protocol liaison to community-based physicians regarding patient referrals for clinical trials in coordination with the ACTU Study Coordinator. Acts as data manager for protocol and prepares new clinical protocol for IRB submission; coordinates and maintains activities to ensure study protocols are carried out effectively and appropriate time frame.
Full-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Assist Clinical Research Investigators with clinical protocol development, preparation and submission of research grants, study proposals, progress reports, posters, manuscripts, and abstracts.
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Operates as part of a team of both nursing staff and research assistants who assist the study coordinator and Investigator in protocol implementation. They assure a smooth implementation of the protocol on the CRU - and that the investigator's research study is implemented according to protocol; and provides - as needed - education to other staff members at the CRU or collaborating institutions, regarding protocols for which she is the provides primary care; and standard of care to non-research patients.
ExpandApply NowActive JobUpdated 12 days ago - UpvoteDownvoteShare Job
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Conduct clinical research according to approved protocols as a study Principal Investigator, Protocol Chair, Associate Investigator, Consultant, or other designated role and maintain ethical and regulatory compliance as well as the integrity of study data and health and welfare of study participants.
Full-timeExpandApply NowActive JobUpdated 27 days ago - UpvoteDownvoteShare Job
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Planning Study start-up, anticipate implementation of protocol amendments, resulting in shifts in study timelines, recruitment and retention challenges, data management and vendor related issues.
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Ad- Hoc Work products and documents related to independent plasmid design, engineering, protocol execution, and validation of Client CRISPR tools - Ad-Hoc Work Details: Independently design, troubleshoot, and carry out various molecular cloning experiments related to CRISPR nterference tool development and iPSC differentiation.
ExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Contributes to the development and Institutional Review Board (IRB) submission of research protocol applications and consent forms on behalf of the study Principal Investigator. HJF is seeking a Research Protocol Coordinator I, II, or III (multiple openings) to support the Murtha Cancer Center Research Program (MCCRP) located at the Rockledge Office in Bethesda, MD. The mission of MCCRP is to improve the diagnosis and multidisciplinary treatment of DoD cancer patients through innovative translational research, evidence-based translational care, and education.
ExpandApply NowActive JobUpdated 12 days ago - UpvoteDownvoteShare Job
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Perform research/regulatory site administrator duties for new clinical protocol including: preparing/coordinating site visit conducted by sponsor/study monitors for study start-up; coordinating study team meetings; addressing questions and requests for documentation from internal and external sources related to the scientific review, development of consents and submission of protocol to NIH IRB; drafting Research Plan for RCA and CRADA (including budget) documents for Tech Transfer office.
Full-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Collaborate with the clinical study team in site identification and selection and assist with study start-up activities; Participate in the development of clinical study protocol concept sheets and protocols, study operations manuals, and other study essential documents.
Full-timeRemoteExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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The Clinical Research Coordinator will be responsible for managing clinical research studies, ensuring protocol compliance, obtaining informed consent from study participants, and coordinating with study sponsors and regulatory agencies.
$47,000 - $60,000 a yearFull-timeExpandApply NowActive JobUpdated 27 days ago - UpvoteDownvoteShare Job
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Candidates are expected to have clinical research oversight expertise in mental health research with the ability to provide expert advice and consultation as needed on NIMH initiatives for clinical research studies and clinical trials including the scope, design, research study operations, human research protections and relevant federal regulation, data and safety monitoring, good clinical practive, and protocol compliance montoring.
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Ensures, reviews, and quality controls against associated project protocol, NIAID requirements, CRF standards templates, Good Clinical Data Management Practices (GCDMP), and where applicable CDISC Clinical Data Acquisition Standards Harmonization (CDASH) standards.
$86,000 - $134,000 a yearFull-timeExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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Work products and documents related to data collection, entry, and analyses from a variety of studies, including presentations and manuscripts; develop and maintain research protocol records; provide consultation regarding study design and use of psychological instruments.
ExpandApply NowActive JobUpdated 10 days ago
protocol study jobs in Falls Church, VA
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