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She/he will be responsible for IRB protocol development, candidate screening, clinical evaluation, coordination of patient follow-up, data collection and analysis, and research project management.
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Has oversight of clinical input to protocol/study team for monitoring guidelines, statistics analysis plans, ICDs, clinical review forms, data edit checks, data quality planning, as needed (ultimately oversees work of protocol/study team.
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The Contractor will utilize knowledge of a broad range of neuro-psychological testing and current literature to advise Government staff on appropriate testing options for achieving the protocol goals.
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Experience developing/implementing integrated security services management processes, such as assessing and auditing network penetration testing, anti–virus planning assistance, risk analysis, and incident response.
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Must have demonstrated knowledge of and experience with common security tools, such as Nessus, NMAP and Wireshark hardware/software security implementation, communication protocol, encryption techniques/tools, and web services.
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Works with Perinatal Outreach team, including Regional Data Coordinator, in perinatal data review, analysis, and presentation. Serves as a resource to affiliate hospitals and community programs on issues related to perinatal clinical policy/protocol, perinatal quality improvement, and perinatal data.
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The specific duties for this position may include protocol development, study design, analysis plan, sample size / power calculations, and interpretation of study data. Assist with grant proposal preparation in study design, sample size calculations, and development of statistical analysis plansQualificationsMaster's degree in biostatistics, statistics or related quantitative field with experience in design, conduct, monitoring, and analysis of cancer clinical studies, in preparing and reviewing clinical trial protocols, and in preparing grant applications and writing research reports, or doctoral degree with experience in these areas.
$100,000 - $115,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Perform system level analysis by conducting simulation, lab measurement and characterization to identify the efficient IO solution in power and routing space constrained HW systems System schematic and MLB layout review and sign off SOC silicon IO specs review and sign off Up to 10% domestic/international travel may be required.
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Act as the lead clinical pharmacologist on clinical pharmacology study teams to support clinical development: independently lead the design, protocol development, execution, analysis, and reporting of clinical pharmacology studies (e.g., food effect, BA/BE, human ADME, drug interactions, renal and hepatic impairment, etc.
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Provide input to protocol design, provide oversight of clinical data (entry by sites, data completeness/accuracy working closely with ClinOps/Biometrics/Data Management teams), and support site and subject retention in clinical trials alongside the Medical Monitor(s.
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The budget specialist is responsible for reviewing the Medicare coverage analysis, protocol, sponsor proposed budget and informed consent (if available) and fully accounting for all clinical costs and investigator and study team effort required to carry out the study, as well as costs for ancillary services.
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Ensures security of HR and Payroll information through established security protocol. Bachelor’s Degree in Computer Science or related field and minimum 6+ years’ experience in a combination of the following areas: application and system development and integration, data modeling/querying/analysis, database management and design, and technical documentation OR High School Diploma and 9+ years’ experience in a combination of the above areas in lieu of a Bachelor’s Degree.
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Study protocol analysis experience, including requirements extraction COA builds and creation / implementation of study design plans. Solid study start-up experience, including having led cross-functional kickoff meetings for EDC, ePRO and/or eCOA activities.
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Leading and/or contributing to the security planning, assessment, risk analysis, risk management, certification and awareness activities for various system and networking operations. Our team of security engineers support enhancements to system security architecture and cyber security capabilities; manage multiple system security plans for development, test and production systems at multiple classification levels following the Risk Management Framework (RMF); manage cross domain capabilities; and support Security Verification Testing (SVT) of relevant Type 1 devices.
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Background knowledge and experience in SIGINT sub-disciplines: COMINT (Communication Externals/COMEXT), ELINT, and Network/Protocol analysis. As Senior Signals Analyst you will be responsible for operating signal collection, processing, and analysis tool suites for exploitation of recordings or live environment; collaborate with analysts throughout the Intelligence Community and maintain awareness of ongoing analysis projects.
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