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The Senior Clinical Trial Manager is accountable for delivery of selected and/or regional activities within a trial (e.g., manage and oversee vendor deliverables, collaborate with functions to set up activities [e.g., DM, IRT, and eRT], support site activation and recruitment, support data review/cleaning activities, support PI/ICF development.
ExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Overview:The role will serve as the “TMF Archivist” and support trial-specific clinical oversight of the TMF as established within Genmab’s procedural documents, GCP-ICH guidelines, and regulatory health expectations during the conduct and closure of the trial.
Full-timeExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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And minimum 7 years global Drug Safety/Pharmacovigilance clinical trial and post marketing experience in a pharmaceutical or biotechnology industry in positions of increasing technical and leadership responsibility.
ExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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Understands clinical trial operational complexities from study start up through enrollment, quality assurance, and study readout. Contributes to the development of brand hallmarks and brand strategy (generic name, brand name, logo, brand colors, positioning, messaging, campaign, segmentation, promotional strategy) understanding the relationship to clinical trial design.
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The Bucks IU Behavior Analysts have the primary responsibility of providing high quality services in the areas of functional behavioral assessment, positive behavior support, verbal behavior, discrete trial, data collection and data analysis, classroom consultation, and staff training.
Full-timeExpandApply NowActive JobUpdated 9 days ago - UpvoteDownvoteShare Job
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Oversees a team and process to ensure ongoing commitments are met across all BMS clinical trials; engages in continuous process improvement to accelerate trial launch and delivery. Will raise awareness of and promote access to clinical trials in a variety of indications while ensuring a focus on diversity and inclusion and driving and accelerating clinical trial recruitment for BMS.
Full-timeExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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Bucks IU Behavior Analysts have the primary responsibility of providing high quality services in the areas of functional behavioral assessment, positive behavior support, verbal behavior, discrete trial, data collection and data analysis, classroom consultation, and staff training.
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Knowledge of clinical and pharmacoeconomic concepts including modeling, real-world evidence, health outcomes and clinical trial designs. Effective Communication: Maintain open and effective communication channels with Medical Strategy, the Global Value and Real-World Evidence (GVRWE) team, Market Access Payer Team, and the MML Team lead to foster partnerships and alignment.
ExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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Through our “Lifecycle Evidence Strategy”, “Clinical Trial Optimization”, “Medical Affairs” and “Real World Evidence” services, we deliver impact where it matters, from early drug development to commercialization.
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Demonstrated understanding of medical terminology and ICH-GCP principles and the application of those principles to trial planning and conduct of clinical trials. Maintains responsibility for quality, performance, regulatory compliance, and patient safety related to managing assigned clinical trial sites and document handling.
ExpandApply NowActive JobUpdated 10 days ago - UpvoteDownvoteShare Job
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Create the budget at study start up, and monitor the overall agreed budget against trial progress. Create the budget at study start up, and monitor the overall agreed budget against trial progress.
ExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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A minimum of 5 years of clinical trial experience within a pharmaceutical, biotechnology, CRO, and/or healthcare setting required; some experience in area of specialty preferred. Attends and participates in trial team meetings Investigator and Monitor Meetings, including but not to limited creating presentations and training site staff.
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Maintains responsibility for quality, performance, regulatory compliance, and patient safety related to managing assigned clinical trials, document management and management of clinical trial management systems and archiving systems.
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The TMF Quality Specialist II will be responsible for maintaining the quality of client Trial Master File integrity and assist in conducting internal and external audits of TMF contents. Plan and coordinate the management of the Trial Master File (TMF) and associated processes, including system and tool development, and business processes documentation.
Full-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Knowledge of the drug development and clinical trial process, including the Product Development and Commercialization Process preferred. At Bristol Myers Squibb, we are inspired by a single vision - transforming patients' lives through science.
ExpandApply NowActive JobUpdated 4 days ago
trial job in Plainsboro, NJ
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