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Have earned at least a Bachelor's degree in the fields of biology, toxicology, chemistry, physics, geospatial science, geography, geosciences, limnology, environmental science, ecology, engineering, computer science, information science, mathematics, bioinformatics, statistics, computational biology, or a related field of study from an accredited university or college within the last 24 months and.
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The Core Laboratory is comprised of multiple testing areas- Chemistry, Toxicology, Blood Gas Analysis, Urinalysis, Coagulation, Automated Hematology and Manual Hematology, including Smear Review and Body Fluid Analysis, and Specimen Processing.
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Work Performed Operations, Study and Site Management – 48% Effort Develop and submit Institutional Review Board [IRB] documents such as consent forms, protocols, and continuing reviews. Maintain study compliance according to institutional requirements, protocols and other applicable policies such as NIH Public Access policy, ct.gov, and Research Data Security Plans.
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Promptly invoice, collect, deposit and record funds to the appropriate fund code according to the executed study budget and payment schedule for study start-up, ongoing per patient revenue, and all other earned invoice able payments.
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1, 2, 3, 4, 5 represents priority rankings, where 1 is highest priority and 5 is lowest priority of those ranked Minimum Education Bachelor Additional Qualifications: Field of Study Biology Computer Science Statistics and Decision Science Software R Python Linux Shiny HTML Skills Scientific Data analysis Data visualization Data processing Data integration Machine learning Apply now.
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Requirements: Master’s degree in biological sciences or related field of study plus 5 years of experience in competitive intelligence, business development marketing, market intelligence, analytics, or related role within the biopharmaceutical/pharmaceutical industry.
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The postdoctoral fellow will participate in existing projects and lead research to study microorganisms especially the microbiome and microbial products of potential aerosol threats and the impact of these insults on the host microbiome.
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Ensures study level ADaM datasets are in compliance with CDISC and regulatory submission requirements, reviews study submission data packages to ensure quality and integrity. Works closely with study leads and Data Management on development of data standards to support data collection requirements; including but not limited to specification of Data transfer agreements (DTAs) in alignment with downstream SDTM and other dataset formats, CRF Standard data collection elements, and external data oversight/strategies to ensure downstream compliance for submission.
$119,400 - $203,100 a yearFull-timeExpandUpdated 3 days ago - UpvoteDownvoteShare Job
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Have earned at least a bachelors degree in biology, toxicology, chemistry, environmental sciences, physics, or closely related field of study from an accredited university or college within the last 24 months and.
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Degree must be within a relevant field: (Biology, Biochemistry, Chemistry, or Toxicology) Masters plus 1 year of relevant experience, or Bachelors plus 3-4 years of relevant experience, No degree requires 7 years of relevant experience.
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Responsible for reviewing the data management documentation, data management plan (DMP), CRF, study database specifications, data validation plan, edit check specifications, data transfer specifications, data issue logs, data review plans and ensures all documents follow study design and regulatory requirements.
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Test utility systems, execute environmental sampling, provide data entry, review data, summarize test results, support performance qualification activities, monitor personnel, Submit LIMS sample rejections, author and summarize re-qualification, performance qualification, and special study protocols, and document control of logbooks.
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The individual will also assist in coordination of specific activities such as method qualification execution, IOQ execution and small study execution. The individual will perform technically diverse testing and analysis with minimal assistance using modern instrumental analytical techniques including but not limited to coagulation assays, enzymatic assays, immunoassays, chromatography (HPLC, GC, IC), capillary electrophoresis, and gel electrophoresis.
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Supervise CRO from study start-up through close-out. The Clinical Trial Manager (CTM) is responsible for the management of clinical trial(s) from vendor selection through Clinical Study Report (CSR) completion.
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Combination of Experience and Education : A combination of specialized work experience equivalent to the next lower grade level AND graduate level education completed in a field of study related to law enforcement (e.g., criminology, criminal justice, law enforcement, courts and judicial systems, corrections and rehabilitation, justice studies, homeland security, forensic technology, and forensic psychology) from an accredited college or university.
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toxicology study jobs in Durham, NC
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