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Home to Princeton University, The Institute for Advanced Study, Princeton Theological Seminary, and an array of cultural centers and organizations, Princeton is regarded as one of the most academically-minded communities in the world.
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Our global Clinical Operations colleagues within our PPD clinical research services provide end-to-end support for clinical trials from study start up to monitoring through to study close out, across commercial and government contracts.
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PPD's centralized monitoring group delivers a new approach to risk surveillance and centralized statistical monitoring, combining the power of statistical and analytical tools with expertise from operationally experienced staff to monitor and manage clinical study data.
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Ensures study systems are complete, accurate and updated per agreed study conventions (e.g. Clinical Trial Management System). With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services.
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Assist Clinical Scientist, Study Responsible Scientist (SRS), &/or Study Responsible Physician (SRP) in various clinical research assigned Immunology Development clinical trials.
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Maintains accurate and complete procedural documentation including study participant and site level documentation in compliance with institutional, local, state and federal guidelines and regulations related to clinical research.
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The CTPN will be primarily responsible for three essential tasks: identifying and connecting patients underrepresented in clinical trials with providers and clinical protocol office study coordinators, clinical trial patient education, and addressing barriers to cancer research participation.
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The Study Implementation Manager is the main interface between our customers and our internal study deployment teams and combines project management, technical and business analysis skills into a key delivery role that supports our goals and ambition to become the leading health-tech provider for clinical studies globally.
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Provides assistance on clinical research studies as per study guidelines and protocols. May be responsible for the following activities: recruiting and evaluating patients for studies; collecting and organizing patient data; scheduling patients for study visits; performing clinical tests such as phlebotomy, EKGs, etc.
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Some studies such as clinical trial in-person focus groups pay as high as $500 per study. Compensation varies per difficulty and length of study. Compensation varies per study.
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This individual should be motivated to participate in the expansion of the Sylvester Comprehensive Cancer Center Clinical Trials portfolio in the study of Breast cancers. This faculty position will have clinical, research and administrative responsibilities within the Department of Medicine, Division of Medical Oncology, and the Sylvester Comprehensive Cancer Center.
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This opportunity is for completing market research opportunities with independent brands via online or phone. Any costs are incurred by the independent market research companies looking to partner with our applicants.
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Thank you for your interest in becoming a Paid Product Tester. Once complete, invitations will reach you via on-site or via email. Each product test is conducted by a third party, independent company.
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Manages study level vendor relationships in conjunction with Clinical Operations. Translates trends in operational and systematic issues and develops solutions with sustainability in mind to ensure roadblocks are removed during study start-up.
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Online studies typically take 15 minutes, while telephone interviews may take 30-60 minutes each session. You are required to complete your profile to be considered for participation. Please complete your profile to view projects available to you.
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