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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.
$143,250 - $210,100 a yearFull-timeExpandApply NowActive JobUpdated 1 month 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.
$190,000 - $280,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Identify and assist, as needed, in initiation and closure of investigator-sponsored clinical trials (ISS). Minimum 2 years Rare Disease MSL experience preferred. Ensure a close working relationship with all US cross-functional Rare Disease team members, including field-based counterparts and home office-based team members, legal, regulatory, market access individuals, medical/clinical operations.
$143,250 - $210,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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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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Competitive salaries are available for qualified candidates at the archaeologist and Principal Investigator levels. Will assist in or direct project planning, proposal writing, research, field work, laboratory work, report preparation, project management, quality assurance and quality control on a wide variety of energy and public utility, real estate and development, historic preservation, and other projects.
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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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In this multifaceted role, the incumbent will provide expert medical and scientific support across the US Endocrinology franchise including formulating US Lifecycle Management for the US franchise including management of Real-World Evidence studies, Investigator-Sponsored Studies (ISS) and any US-based study for the Endocrinology therapeutic area.
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Leads or collaborates on required tasks prior to commencement of clinical trials that include, but are not limited to: clinical planning, protocol development, case report form (CRF) development, IRB submissions, investigator agreements, informed consent form (ICF) development, site selection and communication with clinical trial sites regarding all logistics including contract agreements, support materials and training.
$120,000 - $155,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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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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This position is open to New Jersey Judiciary employees currently holding the permanent title of Investigator or Investigator Bilingual. The New Jersey Judiciary consists of: the Supreme Court, the Superior Court including the Appellate Division and the Trial Court of the 15 vicinages in New Jersey, the Tax Court and the Municipal Court System.
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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.
Full-timeExpandApply NowActive JobUpdated 28 days ago - UpvoteDownvoteShare Job
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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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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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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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dst investigator jobs Company: Metroplus Health Plan in Basking Ridge, NJ
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