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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 - $210,000 a yearFull-timeExpandApply NowActive JobUpdated 5 days 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 10 days 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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Travel to DSD, DSE, DST locations which will include overnight travel. These business functions include: Clinical Operations, Clinical Development, Biostatistics and Data Management, Regulatory Affairs, Quantitative Clinical Pharmacology, Clinical Safety and Pharmacovigilance, Regulatory/Risk Management, Quality Assurance, Medical Affairs, Translational Research, Research, Informatics Services Project Management and Operational Management.
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Experience working with Transfers Agents & Fund Administrators in the Alternatives space (DST, iCapital, State Street, Computershare, etc.) Experience working with Transfers Agents & Fund Administrators in the Alternatives space (DST, iCapital, State Street, Computershare, etc.
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Support the implementation of MA/MS strategies and tactics for HCPs including medical educational activities, grants and investigator-sponsored/collaborative studies and adjust tactical execution as needed.
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Follows-up with the Investigator for additional clinical/medical information or clarifications for AEs and SAEs and provides clinical/medical expertise for safety amendments, Investigator Notifications (INs), Urgent Safety Measures (USM), etc.
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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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Certified Principal Investigator (CPI) Certification. Never resting on our laurels of sourcing candidates thoroughly and presenting our clients only the cream of the crop. Sound knowledge of anatomy, physiology, pathology, and medical terminology.
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Track study metrics such as site start-up, Investigator/site performance, recruitment, regulatory documents, TMF filing and QC activities and elevate areas of concern to your supervisor. This may include preparing meeting logistics, distributing agendas, and minutes for study team meeting, meetings with Academic Research Organizations (AROs), and meetings with CRO and Investigator Meetings.
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The Patient Navigator, reporting to Principal Investigator and Project Director, will monitor Hepatitis B and Hepatitis C screening in the ED, inpatient, and outpatient locations in addition to working with the project implementation team to expand screening programs to other hospital locations and include HIV screening to the program.
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The Grants and Contracts Administrator is also required to submit quarterly expenditure and fiscal reports to granting agencies and lead all financial aspects of the grant program, including providing leadership and guidance at meetings and in communications with the Principal Investigator, the granting agencies, and third-party auditors.
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Contribute labeling perspective 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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Responsible for analyzing data to determine fraud schemes, trends and conducting major case investigations concerning medical and non-medical systemic and organized fraud investigations in all lines of business, including: Auto, Property, General Liability and Workers Compensation.
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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.
$30 - $43 an hourExpandApply NowActive JobUpdated 7 days ago
dst investigator jobs Company: Metroplus Health Plan in Short Hills, NJ
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