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We require a drug-free workplace and require team members to comply with the MMR, Varicella, Tdap, and Influenza vaccine requirement if in an on-site or hybrid workplace category.
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Working to help enroll patients in clinical trials via pharmacy locations 5 days on-site. At Actalent, diversity and inclusion are a bridge towards the equity and success of our people.
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Defines, develops, and implements a plan that addresses and manages the local, state, and federal regulatory and compliance requirements for clinical trials and translational research.
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Looking to hire an individual with a clinical research background to act as the Clinical Research Coordinator for a research site in on a Dermatology clinical trial.
$33 an hourRemoteExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Manages and oversees the day-to-day operations in the administration of clinical trial activities at the site-level (i.e., direct interactions with study participants). Job Title: Senior Clinical Research Coordinator.
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Documents clinical trial findings and examines data accuracy through computer data analysis programs and on-site and remote monitoring. For more than 130 years, diversity, equity & inclusion (DEI) has been a part of our cultural fabric at Johnson & Johnson and woven into how we do business every day.
$166,750 a yearFull-timeExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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As a Clinical Research Coordinator, you will work on-site to facilitate the implementation and conduct of clinical research. Built on the foundation of our Mission and Core Values, we integrate diversity, equity, and inclusion in all that we do.
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Summary: A typical Research Assistant performs a variety of administrative tasks in support of clinical trials and assists in the performance of clinical procedures to collect data on patients enrolled and/or seeking enrollment in clinical studies.
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Research queries and variances, and provide feedback to the site data collector. Verify and/or correct research study information on source documents.
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School of Health and Rehabilitation Science, Office of the Dean. The University of Pittsburgh School of Health and Rehabilitation Sciences (SHRS) is a nationally renowned leader in the field of health care education, research, and clinical practice preparation.
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Develops all applicable consent forms for proposed clinical research trials; maintains oversight and documentation of the informed consent process in accordance with applicable federal regulations, IRB determinations and SAHS legal and institutional requirements.
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Clinical Study Coordinator - Clinical Research (On-Site) Duarte Medical Center seeks a full-time, on-site Clinical Study Coordinator to support oncology clinical trials.
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Must have previous clinical research experience and comfortable working on site 5 days a week! Job Title: Clinical Research Coordinator opportunity in Knoxville, TN.
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Job Title: Clinical Research Coordinator opportunity in Wilmington, NC! Diversity, Equity & Inclusion. Maintaining research records of study activity, including case report forms, drug dispensation records, or other regulatory forms as per FDA guidelines.
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Michigan Medicine is firmly committed to advancing inclusion, diversity, equity, accessibility, and belonging, which are core to the culture and values of the Medical School Office of Research.
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clinical research on site equity and inclusion jobs Title: clinical
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