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Rutgers CINJ at University Hospital in Newark, NJ provides NCI -designated Comprehensive Cancer Center services, such as access to the most advanced Cancer treatment options and clinical trials, to the residents of the greater-Newark region to improve outcomes for patients and their families impacted by Cancer.
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Worked on drug trials that use a biomarker to select patients into the trial, include but not limited to, understand clinical trial assay (CTA) requirements with diagnostic partners, sample testing/shipping regulations in different countries, and CDx development requirements.
ExpandApply NowActive JobUpdated 12 days ago - UpvoteDownvoteShare Job
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Experience with clinical trial assays (CTA) in drug clinical trials in communicating between Diagnostic sponsor and Drug sponsor. Contribute in cross-functional rapid response teams to respond to Clinical Trial Application (CTA) queries on new protocols and protocol amendments in compliance with HA deadlines.
$55 an hourExpandApply NowActive JobUpdated 14 days ago - UpvoteDownvoteShare Job
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This individual will play a role in assisting with the development of histopathology-based assays and exploratory biomarker analysis supporting clinical trials. Translational Molecular Biomarkers (TMB) is responsible for the development and execution of clinical biomarker assays across all therapeutic areas and all phases of clinical development.
$105,500 a yearFull-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Experience with developing regulatory strategies in coordination with clinical plans and marketing objectives." Job Title: Regulatory Studio - Associate Director, Precision Medicine & Digital Health.
$55 an hourExpandApply NowActive JobUpdated 16 days ago - UpvoteDownvoteShare Job
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The Sickle Cell Research Nurse will oversee all sickle cell clinical research trials and research databases. The Sickle Cell Research Nurse is also responsible for overseeing the day-to-day ASH RC Sickle Cell Disease related clinical research operations.
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In addition to delivering the best care, Northwell Health is committed to providing access to exclusive clinical trials, developing groundbreaking treatments, and leading the way in medical research that can change the future of cardiac care.
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Collaborates with cross functional teams (Biostatistics, Clinical Operations, Data Management, Regulatory, PK/ADME, Pharmacovigilance, Commercial) during design, execution, and reporting of early-stage clinical trials.
$264,000 a yearFull-timeRemoteExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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CPD scientists focus on developing safe, economical, sustainable, and robust processes to support clinical trials and the launch of new medicines across various drug modalities including small molecules, peptides, oligonucleotides, and antibody drug conjugates.
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Interpret clinic schedule and protocol into a resource that can be used to identify the date/time to compound/prepare and dispense IP for clinical trials. This individual will be responsible for dispensing Investigational Products (IP) as part of clinical research trials.
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Prior experience in providing MSL-level support to products or devices in endocrinology and/or rare disease, including KOL development, investigator-initiated clinical trials, publications and educational programs, highly preferred.
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Oversight of safety surveillance and pharmacovigilance activities for products in clinical trials and post marketing. Understand MOA in close collaboration with preclinical, clinical pharmacy, clinical development, and discovery.
Full-timeRemoteExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Providing expert input on and ensuring safety tasks in clinical trials (including protocol review, SUSAR, ASR/DSUR, safety reporting, informed consent forms, investigator brochure, unblinding) are handled appropriately and in compliance with regulations as well the design of the study meets the needs for risk management and B/R balance activities.
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As the Director of Trial Master File Operations, you will be responsible for leading the TMF (Trial Master File) operations function for clinical trials across Eikon Therapeutics. The successful candidate will be a strong leader with excellent communication and collaboration skills, and experience in managing TMFs for clinical trials.
$218,500 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Develop quality strategies for new clinical trial technology and approaches (e.g., decentralized trials, real world evidence, digital health, etc.) Oversee the development and maintenance of an effective inspection management framework supporting clinical trials.
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clinical trials jobs in Elizabeth, NJ
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