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We are seeking an experienced NYS-DEP Asbestos Investigator/Project Manager to conduct asbestos-containing materials inspections in a variety of building types in the New York City area. NYSDOL Asbestos Inspector and NYCDEP Asbestos Investigator.
$110,000 a yearFull-timeExpandApply NowActive JobUpdated 20 days ago - UpvoteDownvoteShare Job
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Reviews and validates the study CRF's in conjunction with the Investigator and the Clinical Research Associate of the Study. Assists in transcribing study data from source documents to sponsor designated case report forms or record data for remote data entry, if applicable and resolves data queries in conjunction with the sponsor.
Full-timeExpandApply NowActive JobUpdated 24 days ago - UpvoteDownvoteShare Job
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Collaborate with Translational Scientists, Companion Diagnostic Scientists and Clinical Scientists and Operations Leads in the review of clinical protocols, laboratory instructions, investigator training, clinical sample analysis, archiving of biomarker test results, and regulatory submission activities for Daiichi Sankyo clinical development.
Full-timeExpandApply NowActive JobUpdated 20 days ago - UpvoteDownvoteShare Job
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The primary responsibility of the Rare Disease Medical Science Liaison (MSL) is to act as a liaison with nationwide and regional thought leaders (TLs) to align interests, discuss research and medical information, and to facilitate both clinical trial efforts of Ipsen and Investigator-sponsored studies.
Full-timeExpandApply NowActive JobUpdated 20 days ago - UpvoteDownvoteShare Job
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Identify and assist, as needed, in initiation and closure of investigator-sponsored clinical trials (ISS). Medical Science Liaison, Rare Disease, Liver (MI, OH, IN) Minimum 2 years Rare Disease MSL experience preferred.
$210,100 a yearFull-timeExpandApply NowActive JobUpdated 2 months ago - UpvoteDownvoteShare Job
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Successfully answering these questions will require the design of research that is fit for purpose (including pharmacoepidemiology research, registries, Health Economics and Outcomes Research (HEOR), oversight of investigator-initiated research plan, etc.
$280,000 a yearFull-timeExpandApply NowActive JobUpdated 20 days ago - UpvoteDownvoteShare Job
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Coordinates pediatric projects across oncology, including both BMS sponsored, as well as investigator sponsored research projects and trials, and compassionate use programs. The Clinical Development Lead Pediatric Hematology, Oncology and Cell Therapy sits within Clinical Development, which is a global organization dedicated to the effective design and execution of drug development.
Full-timeExpandApply NowActive JobUpdated 18 days ago - UpvoteDownvoteShare Job
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Informs Investigator Initiated Study (IIS) strategy and can act as Docent for IISs. Represents AbbVie at external meetings including investigator meetings, scientific association meetings, etc.
Full-timeExpandApply NowActive JobUpdated 22 days ago - UpvoteDownvoteShare Job
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Perform GCP audits (e.g., CRO, vendor, investigator site, TMF) and manage the GCP audit process for self-performed audits and outsourced audits. This role is crucial for ensuring quality oversight of clinical studies and vendor programs, maintaining compliance with ICH GCP and FDA regulatory requirements, and upholding our high standards for data integrity.
Full-timeExpandApply NowActive JobUpdated 10 days ago - UpvoteDownvoteShare Job
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Monitors and updates investigator/site status for the trial, and supports with clinical trial registry postings. Collates materials for training and investigator meetings. Performs scheduled reconciliations of study Trial Master File (TMF) with clinical study lead guidance.
$62.5 an hourExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Experienced SIU field investigator will also be considered who meet qualifications listed. Experienced SIU field investigator will also be considered who meet qualifications listed. SIU affiliated professional designation preferred (FCLS,SCLA, CFE, CIFI.
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Deliverables may include sections of individual protocols consistent with the clinical development plan (CDP), data review, program specific standards, clinical components of regulatory documents/registration dossiers, and publications (e.g., investigator brochures, briefing books, safety updates, submission dossiers, and responses to health authorities.
Full-timeExpandApply NowActive JobUpdated 9 days ago - UpvoteDownvoteShare Job
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As a Barclays Financial Intelligence Unit Investigator AVP, you will be responsible for the investigation and regulatory reporting of complex and priority financial crime threats. As a Barclays Financial Intelligence Unit Investigator AVP, you will be responsible for the investigation and regulatory reporting of complex and priority financial crime threats.
Full-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The incumbent also advises the SAC on program matters, and coordinates evaluations, activities, investigative needs, and other administrative and law enforcement matters through the Criminal Investigation function, other areas within the Service, and with other agencies.
$191,900 a yearExpandApply NowActive JobUpdated 20 days ago - UpvoteDownvoteShare Job
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The Sr Clinical Investigator, CRS oversees the clinical research of consumer products involving healthy paid volunteers. Notifies the Sponsor and the IRB about Adverse Events (AEs), Serious Adverse Events (SAEs) and Adverse Reactions (ARs.
Full-timeExpandApply NowActive JobUpdated 24 days ago
investigator job Company: Metroplus Health Plan in Madison, NJ
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