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4 or More Years More than 5 years of experience in imaging operations in oncology clinical development of both early and late phase clinical trials, including development and review of imaging section of the protocol, imaging charter, site manuals, and communication plan •Deep knowledge of implementation of oncology tumor assessment performed by (1) investigator/site and (2) BICR for both solid tumors and hematological malignancy.
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Experience in the clinical drug development process, specifically trial planning and execution practices, including IRB/IEC and Investigator site roles and responsibilities. Review investigator site essential documentation packages from CROs per process and sample as needed.
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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 - $286,000 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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A combination of the following certifications: NYCDEP Asbestos Investigator EPA AHERA / NYSDOL Asbestos Inspector, Project Designer, Project Monitor and Air Sampling Technician NJ/EPA/NY Lead Risk Assessor/Inspector NYSDOL Mold Assessor.
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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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You will develop and execute the U.S. Medical and Scientific Affairs strategy and execution, policies, programs and SOPs; oversee Investigator Sponsored Trial (IST) programs. You have the power to build, manage, and develop a team of highly competent and engaged managers in the areas of Medical and Scientific Affairs, Medical Information and Pharmacovigilance.
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Collaborate with MSL colleagues to ensure all Investigator sponsored studies are performed according to legal/regulatory guidelines. Supports the team in the tracking and compliance of US Investigator Sponsored Studies across franchises.
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Under direction, the Investigator or Trainee performs sanitary inspection and environmental health work involving in the enforcement of relevant sanitary, environmental, and public health laws and rules within Morris County; conducts inspections, investigations, and educational outreach activities; performs other related duties as required and/or necessary.
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As a Loss Prevention Investigator, you will be working as a member of our Loss Prevention team to prevent losses from external and internal theft and fraud, reporting to the Assistant Loss Prevention Manager and Senior Retail Performance and Store Operations Manager.
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Participate in training opportunities to advance knowledge of drug development and Good Clinical Practice Guidelines Support company's visibility and position with the CRO industry through publications and presentations Develop new and enhances existing client/investigator relationships whenever possible Participate in process improvement activities for company.
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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.
Full-timeExpandApply NowActive JobUpdated 10 days ago - UpvoteDownvoteShare Job
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Description :Develop strategy and tactics for an integrated Medical Plan (Medical Science Liaisons, Medical Education, Medical Communications and Publications, Health Outcomes, Safety and Clinical Research (Phase IIIB-IV and Investigator Sponsored Trials) and annual budget for assignedimmunology products.
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Develop strategy and tactics for an integrated Medical Plan (Medical Science Liaisons, Medical Education, Medical Communications and Publications, Health Outcomes, Safety and Clinical Research (Phase IIIB-IV and Investigator Sponsored Trials) and annual budget across immunology pipeline.
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MD, PhD, MPH, PharmD, RN or PA with at least 5 years’ experience in Epidemiology, Health Economics Outcomes Research (HEOR), or/and Health Systems Research. with partnerships from other parts of Medical Affairs, Publications and Scientific Communications, Pharmacovigilance, Clinical Development, Market Access, and Commercial functions.
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Facilitate the review and evaluation of Serious Adverse Reactions for inclusion in the Investigator Brochure Reference Safety Information (IB RSI), including presentation to SMT to ensure alignment.
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investigator job in Basking Ridge, NJ
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