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Meet with patients during designated study visits to perform assessments, including physical examinations and data collection.
$60 an hourExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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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.
ExpandApply NowActive JobUpdated 15 days ago - UpvoteDownvoteShare Job
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We are seeking a Patient Recruitment Specialist to join our dynamic and growing clinical research team!
Full-timeExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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Recruit and screen subjects for clinical trials and maintain all logs. Company Description WE ARE A GROWING COMPANY WITH VARIOUS DOCTORS SERVING AS PI IN DIFFERENT AREAS OF PRACTICE. WE SPECIALIZE IN CLINICAL TRIALS WE DO NOT OFFER REGULAR MEDICAL SERVICES.
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Senior Project Manager / Associate Director - CNS / Neuroscience - Latin America OR USA - Home Based
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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.
Work from homeExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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We are Worldwide Clinical Trials, and we are a global team of over 3,000 experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs - in the best possible way.
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Experience in CNS or Rare Disease is required. 5+ years of experience as a Clinical Research Associate. 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.
Full-timeExpandApply NowActive JobUpdated 22 days ago - UpvoteDownvoteShare Job
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An understanding of clinical trials, healthcare, or a related industry. The goal of the Community Outreach Specialist (COS) is to increase awareness and education of clinical research in the community by conducting outreach and engagement initiatives.
Full-timeExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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Community Outreach Specialist Position Overview. Under the direction of marketing and community engagement leadership, the COS will be responsible for the day-to-day operations of all community outreach, education and engagement activities related to a variety of clinical research trials.
ExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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We are actively seeking a Bilingual Community Liaison to join our Viera team. Works with marketing and community engagement team to make recommendations in the community to generate leads for active research studies.
ExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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Achieve individual revenue and sales objectives through proactive communication and sales for Worldwide Clinical Trials early phase services to assigned clients. The Sr. Director of Business Development, Early Phase will be located in the Northeast US geographic region and will be responsible for driving exposure and business growth to our Phase 1 (CPU) Clinical Pharmacology Unite and Bioanalytical Lab capabilities and offerings along with growing new relationships with clients.
RemoteExpandApply NowActive JobUpdated 10 days ago - UpvoteDownvoteShare Job
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The QA Audit Manager will have proven experience and advanced knowledge in appropriate GCP/GxP compliance and other applicable regulations to conduct various types of audits to assessWorldwide Clinical Trials processes and procedures, applicable regulations, and Sponsor SOPs, when necessary.
Full-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Required: Bachelor’s degree preferably in life science and a minimum of five years’ experience in regulatory affairs, auditing, clinical research, monitoring, laboratory, or other relevant area, three (3) of those years must be in quality assurance auditing.
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What the QA Manager does at Worldwide. Sound knowledge of applicable GCP/GxP regulations and requirements as well as WCT policies and procedures. We’re a global, midsize CRO that pushes boundaries, innovates, and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe.
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We are seeking a motivated person who is either a licensed RN, LVN, Medical Assistant or with 3 years of research experience, who can work independently in different research sites and studies.
ExpandApply NowActive JobUpdated 11 days ago
Company: Clinical Trials in United-states, United States
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