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In executing these position responsibilities, the Clinical Research Coordinator is guided by FDA regulations, Good Clinical Practice (GCP), and company standard operating procedures and policies.
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This affiliation has consolidated the clinical, teaching, research and public service programs of the UCSD School of Medicine's Department of Pediatrics with San Diego's only health care system dedicated to the health and well-being of children.
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Founded in 2004, Pharmaron has invested in its people and facilities, and established a broad spectrum of research, development and manufacturing service capabilities throughout the entire drug discovery, preclinical and clinical development process across multiple therapeutic modalities, including small molecules, biologics and CGT products.
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Assist Clinical Scientist, Study Responsible Scientist (SRS), &/or Study Responsible Physician (SRP) in various clinical research assigned Immunology Development clinical trials.
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Control (QC) functions of the SOCCI Clinical Research Office (CRO) to include industry sponsored studies, investigator-initiated studies, and cancer cooperative group trials. Working Title : Clinical Research Specialist II, CCTO (Hybrid.
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Under supervision of the lab manager and lead investigator, performs clinical research work for clinical trials focused on treating posttraumatic stress disorder (PTSD) and related problems (e.
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Responsible for assisting with data collection, ensuring protocol compliance, reporting of adverse drug reactions and follow-up of those events with the Principal Investigator, laboratory and specimen handling (blood & urine), and maintenance of accurate and complete clinical research files.
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Incumbent will lead and provide guidance to clinical monitors for sponsor and investigator initiated clinical research studies. The USC Keck School of Medicine - Alzheimer Therapeutic Research Institute (ATRI), located in San Diego, California is an academic institute comprised of an expert panel of scientific collaborators committed to advancing the development of new treatments for Alzheimer's Disease (AD) through innovative clinical trials.
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Artemis Research is a leading principal investigator- and patient-focused clinical research company dedicated to advancing medical treatments. Under the supervision of the Site Director, the Clinical Research Coordinator I is responsible for the conduct of research protocols, such that the integrity and quality of the clinical research is maintained and the research is conducted in accordance with Good Clinical Practice Guidelines.
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Your responsibilities will encompass overseeing all aspects of Clinical Quality, managing external Contract Research Organizations (CROs), and providing additional support for internal quality systems.
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Provide study management by interfacing with representatives from key functional groups such as: Clinical Development, Data Management, Statistics, Regulatory Affairs, QA, Medical Writing, CMC, and Research.
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Familiarity with concepts of clinical research and clinical trial design, including biostatistics. 2 to 10 years experience in pharmaceutical and/or biotechnology industry developing investigational new drugs or experience in a clinical research organization involved in clinical trials.
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The Clinical Quality Associate Director will be responsible all aspects of Clinical Quality, oversee external Contract Research Organizations (CROs), and provide additional support for the Tr1X internal quality systems.
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Incumbent will provide oversight to the progress of clinical trials at study sites, and ensure that they are conducted, recorded, and reported in accordance with the protocol, Standard Operating Procedures (SOPs), Good Clinical Practice (GCP), and the applicable regulatory requirement(s.
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Respond to customer needs and complaints regarding products and service by developing creative and feasible solutions or working with other related personnel (e.g., sales managers, clinical research, marketing, technical support) to develop optimal solutions.
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clinical research investigator jobs in San Diego, CA
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