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Monitors and updates investigator/site status for the trial, and supports with clinical trial registry postings. Trial Master File reconciliations; manages and maintains the eTMF, ensures scheduled reports are received (1572, re-portable changes, financial disclosures), Tracks and monitors close out activities – study close-out documents (1572s, Investigational Product reconciliation, Financial Disclosures, etc.
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As a Wage and Hour Investigator at the grades GS-7 through the GS-11, you will receive on-the-job and other formal training related to the provisions of the laws enforced by the agency. Industrial personnel or salary and wage administration or responsible work in a certified public accounting firm.
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HDI Desktop Support Technician (HDI-DST) a plus. HDI Desktop Support Technician (HDI-DST) a plus. The Senior Technician, Desktop Support will act as a technical escalation focal to the Desktop Support Technician I and II positions but will not have any supervisory authority.
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Experience working with DST Systems / iCapital / State Street. Assist in the communication of capital events to key distribution relationships and financial advisors. Experience working with DST Systems / iCapital / State Street.
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Working in collaboration with the Principal Investigator, the Sr. CRC is responsible for the oversight, facilitation and coordination of the daily clinical trial activities and plays a critical role in the conduct of the study.
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Experience in supporting post-approval studies/ clinical trials, including observational studies, PMR/PASS/PAES type of studies, disease/treatment registry type of studies, investigator-initiated studies/trials, and assessments of electronic health records like claims databases and preparation of health technology assessment (HTA) dossiers.
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Elevance Health Lead Investigator Morristown , New Jersey Apply Now WARNING: Please beware of phishing scams that solicit interviews or promote work-at-home opportunities, some of which may pose as legitimate companies.
$87,024 - $149,184 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Contributes from the labeling perspective/labeling environment to Clinical Study designs, protocols, Investigator Brochures and Briefing Books." Knowledge of Global Labeling Guidances, Drug Development and Commercialization of prescription medicines.
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Evaluate Investigator Sponsored Research (ISR), participates in Clinical Trials Review Process and is accountable for activities related to approved ISRs. Contribute to, review, and approve medical/scientific communications including marketing materials and participate in Promotional and Scientific Content Approval Processes.
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Assist the research scientist or supervising principal investigator with ongoing research studies based on the research protocols, including subject recruitment, data collection, database entry and management, statistical analysis and administrative duties.
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IAAI Certified Fire Investigator (IAAI-CFI) certification is preferred. Minimum certification requirement for consideration, Certified Fire & Explosion Investigator (CFEI). Promotes and markets utilization of EFI services in the insurance industry and within assigned territory Serves as a liaison between the insurance industry and law enforcement/fire service personnel.
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O Knowledge of Global Labeling Guidances, Drug Development and Commercialization of prescription medicines. Serves as primary contact for cross-functional Labeling Team Member (CFLT), eg Global Regulatory Team Lead (GRTL), Medical Surveillance Team Lead (MSTL), Functional SMEs, Documentation Leads and Medical Writer, Dossier Lead and Submission Manager, also serves as interface for Country Regulatory Managers to support timely and quality submissions globally.
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Performs other duties related to the clinical trials as delegated by the Principal Investigator. Maintain regular contact with the Principal Investigator and team to review study details (e.g., progress, adverse events, enrolment.
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Coordinating the preparation of clinical study reports, investigator brochures, and other regulatory documents relevant to rare disease clinical trials. Establishing and maintaining relationships with Key Opinion Leaders (KOLs), external experts in the field of rare diseases to gather insights, facilitate investigator-initiated studies, and advance scientific knowledge.
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Contribute labeling perspective to Clinical Study designs, protocols, Investigator Brochures, and Briefing Books. Contribute labeling perspective to Clinical Study designs, protocols, Investigator Brochures, and Briefing Books.
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dst investigator jobs Company: Metroplus Health Plan in Short Hills, NJ
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