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NCH is transforming into an Advanced Community Healthcare System(TM) and we’re proud to: Provide higher acuity care and Centers of Excellence; Offer Graduate Medical Education and fellowships; Have endowed chairs; Conduct research and participate in national clinical trials; and partner with other health market leaders, like Hospital for Special Surgery, Encompass, and ProScan.
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Reporting to the Chief Technology Officer, the Senior Manager/Associate Director of Clinical GCP Quality will be responsible for evaluating and mitigating risk of global clinical development programs, from initiation through completion of clinical trials, with inspection readiness in mind throughout.
Full-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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The practice is actively involved in research and currently involved in multiple clinical trials. State of the art cardiology office with top tier diagnostic equipment including nuclear, echo, and vascular accreditation.
$400,000 a yearFull-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Provide internal safety monitoring for clinical trials in collaboration with the Study Medical Director and Drug Safety team. 5+ years of experience in the design and conduct of autoimmune clinical trials.
$240,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Programs SAS edit checks and SAS macros for clinical trials, encompassing ETL processes, data validations, statistical analyses, and report generation. Responsible for data management activities including, but not limited to, developing data management plans, department SOPs, supervising and performing database development, testing, validation, reviewing and processing clinical trial data to ensure the completeness, accuracy and consistency of clinical trials databases.
$75 an hourExpandApply NowActive JobUpdated 12 days ago - UpvoteDownvoteShare Job
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Incumbents work under supervision of Clinical Shift Supervisor and/or Clinical Research Coordinator (assigned to study), performing routine duties and referring questions and problems to the supervisor.
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Knowledge of basic biological principles and the pharmaceutical development process (including clinical trials, patient level datasets and study documentation) Clean, harmonize, curate and catalog clinical, omics, and other data and metadata according to various data practices and standards.
$175,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Educational and research opportunities are actively offered and supported, with residency programs and fellowships, along with participation in clinical studies and trials. San Diego maintains a high level of integration and collaboration; physicians and new hires alike know they’re not alone, that they have the personal support and clinical assistance of an entire team.
$110 - $136.44InternExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Facilitate education & information concerning all ongoing clinical trials as well as training & monitoring research staff assigned to these protocols. The position requires demonstrated leadership skills and vast knowledge of clinical data, data registries, & clinical research activities related to pediatric hematology and oncology.
$76.45 an hourFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Develop and execute SAS macros and programs for clinical trials, encompassing ETL processes, data validations, statistical analyses, and report generation. Clinical trial in EDC.
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4 years clinical trials experience as Medical Assistant or Lab technician. Responsible for planning, implementation and oversight of a variety of clinical trials, maintains compliance with all applicable institutional, state and federal regulations in collaboration with investigator.
$52.91 an hourFull-timeExpandApply NowActive JobUpdated 16 days ago - UpvoteDownvoteShare Job
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Design clinical trials and review critical study documents (e.g., Investigator Brochures, IND submissions). 8+ years of clinical research experience in the pharmaceutical industry.
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Under the supervision of the Site Director, the Research Assistant will be responsible for supporting various activities associated with the day-to-day operations of the research department in the conduct of clinical trials in psychiatry and internal medicine.
$22 an hourFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Job Title: Clinical Research AssociateJob DescriptionSeeking a proactive and diligent Clinical Research Associate (CRA) to manage all aspects of clinical trials from monitoring to close-out.
$38 - $58 an hourExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Responsible for design and medical oversight of clinical trials activities in partnership with relevant cross-functional stakeholders (Clinical Operations, Biometrics and Data Management, Regulatory, Drug Safety and Pharmacovigilance.
$325,075 a yearFull-timeExpandApply NowActive JobUpdated 2 days ago
clinical trials jobs in La Jolla, CA
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