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Meet with patients during designated study visits to perform assessments, including physical examinations and data collection.
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Always represents Worldwide Clinical Trials (WCT) in a professional manner (verbal written and in appearance) when interacting with Sponsors, subjects, outside vendors and fellow employees.
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Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications – from discovery to reality.
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SUMMARY: The Operations Manager has primary responsibility for overseeing the operational work related to rater selection, rater certification/qualification, rater training content, scale acquisition, surveillance maintenance, and workbook/source document for Worldwide Clinical Trials, Inc. (Worldwide.
Full-timeExpandApply NowActive JobUpdated 15 days ago - UpvoteDownvoteShare Job
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Simplify Clinical Trials is dedicated to revolutionizing the clinical research industry by developing innovative solutions to address data-related challenges. Our unique approach streamlines data management processes, enhancing the efficiency and accuracy of clinical trials.
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Through efforts of the Foundation in support of the Alliance, clinical trials and laboratory research are conducted to discover new or improved ways to prevent, treat, and cure many types of cancer, including leukemia and lymphoma, and cancers of the breast, prostate, lung, and gastrointestinal (GI) tract, and help educate the medical community on methods of cancer diagnosis, treatment, and prevention.
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We conduct clinical trials with various pharmaceutical companies in a variety of therapeutic areas, including but not limited to, internal medicine, dermatology, neurology, pulmonology, cardiology, psychiatry, endocrinology, and gastroenterology.
$91,000 a yearFull-timeExpandApply NowActive JobUpdated 15 days ago - UpvoteDownvoteShare Job
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Because all these functions are directly related to the vision of The Clinical Trials Network (CTNx) this position will report to the Chief Operating Officer (COO). The Clinical Trials Network (CTNx) is a trial management company that oversees a network of private practice clinical research sites with a unique approach to streamlining the administrative, regulatory, and compliance aspects of conducting clinical trials.
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The PRN Medical Writer is responsible for carrying out medical writing activities in accordance with client specifications in a timely, accurate, and efficient manner, within budget and to the written, scientific, and ethical standards in accordance with regulatory requirements and WCT standard operating procedures (SOPs.
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5+ years of experience as a Clinical Research Associate. Experience in Rare Disease/Respiratory is required. 4-year university degree or RN/BSN in Nursing. Join our Neuroscience team, who provides expertise in Alzheimer's Disease & Dementia, Neurology, Pain, Psychiatry and Psychedelics.
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Anchored in our company’s scientific heritage, our dedicated therapeutic focus on cardiovascular, metabolic, neuroscience, oncology, and rare diseases, is applied to develop flexible plans and solve problems quickly for our customers.
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Proficiency in Microsoft Office, CTMS and EDC Systems. We’re a global, mid-size CRO that pushes boundaries, innovates and invents — because the path to a cure for the world’s most persist diseases is not paved by those who play it safe, but by those who take pioneering, creative approaches, and implement them with quality and excellence.
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These roles are the backbone of every strong CRO, helping drive breakthrough scientific research and playing a lead role on every clinical trial. Clinical Research Associates (CRAs) play a vital role in ensuring our clinical research programs are executed with the quality and excellence our sponsors expect and the care and passion patients deserve.
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Responsible for managing the research activities at sites participating in Worldwide’s clinical research projects, which are predominantly registries and other types of non-interventional / observational studies.
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Performs all job responsibilities in accordance with standards of GCP (Good Clinical Practice), clinic SOPs, OSHA guidelines, Federal and local regulations
Full-timeExpandUpdated 4 days ago
Company: Clinical Trials in California, Maryland
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