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Must have at least 5 years’ experience in fit-for-purpose clinical biomarker assay development, validation, and implementation in support of multi-site clinical trials. The primary responsibilities of this position are 1) to ensure the timely execution of biomarker tests on samples from clinical trials and 2) to perform technical and strategic assessment of new and innovative biomarker platforms.
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The well-rounded and all-inclusive fellowship experience includes participation in services such as palliative care, survivor ship, integrative medicine and clinical trials. The clinical rotations provide fellows with both solid and hematologic malignancy encounters simultaneously.
$74.51 an hourFull-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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At each of our 12 multidisciplinary disease site centers, patients have a fully dedicated team that include oncologists, surgeons, navigators, and social workers, as well as a clinical research nurse at each MDC to explore avenues for potential cutting-edge treatments in the latest clinical trials.
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Supports IRB approved clinical research/trials though a variety of activities including but not limited to: obtaining consent; ordering diagnostic tests; recording laboratory and diagnostic results; administering therapeutic interventions; and documenting and reporting patient outcomes including toxicities or adverse events.
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ADDITIONAL JOB RESPONSIBILITIES:The Clinical Research Coordinator handles or assists with the administrative activities generally associated with the conduct of clinical trials and mixed methods research specific to LGBTQ+ populations.
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Keywords : senior director, clinical program lead, late-stage clinical development, clinical trials, global, strategy, hematology, lymphoma, oncology, targeted therapies, ADCs, antibody-drug conjugates, program, asset, label extension, life-cycle management, pharma, biotech, biopharma, MD, medical doctor, phase I, phase II, phase III, FDA.
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The Clinical Research Associate (CRA) will support successful and timely start-up and completion of clinical trials and be a key member of the Organization of Chief Medical Officer (OCMO) Global Clinical Affairs team.
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The Emory Winship Cancer Institute NP/PA Fellowship Program is a one-year program that prepares fellows to become highly skilled in the multidisciplinary, collaborative and evidence-based management of complex and challenging patients in medical oncology and hematology, bone marrow transplant and radiation oncology.
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Position Overview: As a Principal Statistical Programmer with a specialized focus on PK/PD, you will play a pivotal role in the design, execution, and analysis of clinical trials to support the development of our promising drug candidates.
$203,100 a yearFull-timeExpandApply NowActive JobUpdated 21 days ago - UpvoteDownvoteShare Job
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Serves as a clinical expert and education consultant to nursing, members of the healthcare team and to the larger community. Performs approved therapeutic or diagnostic procedures based upon patients clinical status and documents procedures in accordance with hospital requirements, including obtaining arterial, venous, and capillary blood samples, urine samples, sputum samples and cultures; performing cardiac output measurements, other hemodynamic measurements and EKGs; assisting with the performance of radiographic studies; assisting physician with diagnostic and therapeutic procedures; etc.
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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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Our global Clinical Operations colleagues within our PPD® clinical research services provide end-to-end support for clinical trials from study start up to monitoring through to study close out, across commercial and government contracts.
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This is a hands-on role that will utilize your extensive technical expertise and experience to provide recommendations on statistical issues, design and conduct of clinical trials of all phases.
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Lead research in clinical trials, advanced technologies and robotic surgical innovations. Clinical role with admin responsibilities (70-80% clinical/perform surgeries and see patients) with (20-30% administrative role.
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Conduct and manage clinical trials in accordance with the study protocol, GCP, ICH Guidelines and SOPs. Implement and coordinate assigned clinical trials including start up, vendor management, subject recruitment, source development review, scheduling subjects, protocol training, collection of regulatory documents, conducting visits, ensuring data is entered in a timely manner and all queries are resolved, managing, and reporting adverse events, serious adverse events, and deviations, implementing new protocol amendments, providing all close out reports.
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clinical trials jobs in Georgia, GA
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