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The Clinical Research Nurse carries out the research and works under the general supervision of the principal investigator responsible for the clinical trials. The Clinical Research Nurse is responsible for coordinating and overseeing clinical research operations for all assigned clinical trials and participates in assessing, planning, implementing and evaluating Compliant Patient Care in clinical research trials.
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QP2 provides mathematical modeling, simulation, and pharmacokinetic / pharmacodynamic (PK/PD) analysis to enable drug development decisions across the pipeline – starting at discovery / preclinical investigation, through early-stage clinical trials, to late-stage clinical trials and drug registration.
$105,500 a yearFull-timeExpandApply NowActive JobUpdated 17 days ago - UpvoteDownvoteShare Job
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Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market.
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The practice offers Hematology/Medical Oncology, Breast Surgery, Palliative Care, Radiation Oncology, and Clinical Trials & Research Programs. OneOncology’s non-exclusive clinical trial site management subsidiary, OneR, delivers complex, multi-center clinical trials to affiliated practices.
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Phase 1, 2, and 3 clinical trials. Their team of multidisciplinary experts works together to improve the patient experience and provide efficient access to care, minimizing the clinical, financial, and emotional barriers that patients face.
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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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Katalyst Healthcares & Life Sciences is hiring entry level candidates for several positions for contract research in Clinical trials of drugs, biologics and medical devices. We have a few immediate job opportunities available in Drug Safety and Pharmacovigilance and Clinical Research field.
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The position is responsible for implementation and management of system to manage quality throughout all stages of clinical trials and will report to the Vice President of Clinical Operations within the Chief Medical Officer (CMO) organization.
$230,000 a yearExpandApply NowActive JobUpdated 12 days ago - UpvoteDownvoteShare Job
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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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Solid understanding of clinical research methods, Clinical Data Interchange Standards Consortium (CDISC) principles, best data management practices and technologies related to clinical trials.
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The Global Clinical Supply (GCS) organization is accountable for managing the 'end-to-end' integrated clinical supply chain across the full company Research Laboratories (Research and Development Division) portfolio of clinical trials.
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The Program Clinical Supplies Project Manager (Program CSPM) serves as the primary program-level GCS point of contact representing the GCS Planning organization to customers both internal and external to GCS and serves as the lead GCS spokesperson at clinical and development related meetings.
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Ability to Enroll Patients in Clinical Trials. Our team of multidisciplinary experts works together to improve the patient's experience and provide efficient access to care, minimizing the clinical, financial, and emotional barriers that patients face.
Full-timeExpandApply NowActive JobUpdated 2 months ago - UpvoteDownvoteShare Job
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The student should have a strong interest in clinical trials administration and drug discovery process. Primary responsibilities will include assisting clinical trials teams with the planning, execution and/or close out of a clinical trial(s.
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Clinical Trials Payment Coordinator/Site payment coordinator. Minimum High school diploma with 3 years of clinical trial site payment experience. BS/BA or Master's degree with with 1-3 years of clinical trial site payment experience is preferred.
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clinical trials jobs in Rahway, NJ
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