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This role involves negotiating complex standalone commercial transactions that advance technologies through clinical trials and toward FDA regulatory approval. Requirements:Juris Doctor (JD) degree from an accredited law school.
Full-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Minimum of 8 years of research development experience with emphasis on managing complex pre and post award grant administration projects relative to human clinical trials in a research consortium setting.
ExpandApply NowActive JobUpdated 3 days 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.
Full-timeExpandApply NowActive JobUpdated 17 days ago - UpvoteDownvoteShare Job
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Reach out to the many groups funding clinical trials in therapeutic ultrasound, diffuse correlation spectroscopy, biophotonics / FNIRS and the ilk to make them aware of our work. a background in therapeutic or focused ultrasound and/or biophotonics and decentralized clinical trials + strong writing, web and sales skills.
ExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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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.
Full-timeRemoteExpandApply NowActive JobUpdated 14 days ago - UpvoteDownvoteShare Job
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Frontage Laboratories Inc. is an award winning, publicly listed (HKSE), full-service CRO/Contract Research Organization operating over 25 state-of-the-art laboratories across the US, Canada and China, and growing over 30% YOY. Our core competencies include drug metabolism, pharmacokinetics/ pharmacodynamics (PK/PD), safety and toxicology, bioanalytical services, chemistry and manufacturing controls for drug development, and core laboratory services for clinical trials.
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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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Innovate Trial Methodologies: Drive the integration of in silico trials, decentralized clinical trials, and digital health technologies to enhance the efficiency and reach of clinical studies, ensuring robust data collection and patient accessibility.
$258,000 a yearFull-timeExpandApply NowActive JobUpdated 9 days ago - UpvoteDownvoteShare Job
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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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3+ years of Oncology clinical trials experience as a Clinical Research Coordinator (CRC) including experience(s) with an Investigational New Drug (IND) or Investigational Product (IP.
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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.
Full-timeExpandApply NowActive JobUpdated 14 days ago - UpvoteDownvoteShare Job
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Experience with Clinical Trials Data in a pharma/life science industry is a strong plus. The Data Visualization Engineer will work in Daiichi Sankyo IT – MARS Team. We believe in providing staffing solutions to address the current talent gap – Right Talent – Right Time – Right Place – Right Price and acting as a Career Coach to our consultants.
ExpandApply NowActive JobUpdated 8 days 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.
Full-timeExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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Must be fully cognizant and adhere to regulatory and legal (Business Conduct) requirements for clinical trials and other Medical Affairs activities; thorough knowledge of FDA regulations, ICH guidelines and GCPs governing the conduct of clinical trials.
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Ensure clinical trials are conducted in accordance with the protocol, standard operating procedures, ICH/GCP, and all applicable regulatory requirements. The Clinical Trial Assistant will assist with the review, tracking and monitoring the day-to-day aspects of clinical trials at investigative sites and ensure clinical trial(s) documentation is collected, recorded, and filed.
ExpandApply NowActive JobUpdated 10 days ago
clinical trials jobs in Newark, NJ
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