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We are looking for a self-directed professional support Digital Health Technology [DHT] (wearable sensors) and imaging components set-up and monitoring within clinical trials; specifically focused on the operational initiation/set-up, vendor and digital data/imaging monitoring, and data cleaning process efforts that occur within the Bio measures Endpoints and Study Technologies (BEST) projects.
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The role represents the CPQP function on drug development teams, leads CPQP sub-teams, and owns strategy and delivery on posology for early and late-stage clinical trials while collaborating with clinicians, clinical operations, bioanalytical, biomarker, pharmacovigilance, regulatory and CMC groups.
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Keywords: Biostatistician, Biostatistics, Principal Biostatistician, Statistician, Statistics, Biostat, Biostats, Clinical Research, Research, Datasets, CRF, Statistical Analysis, Data Analysis, Study Design, Trial Design, SAS, CDISC, ISS, ISE. TLG, TLF, Clinical Trial Data, Data Management, Clinical Trials, Clinical Team, Pharmaceutical, Biopharmaceutical, Pharma, Biopharma, Therapeutics, Biological, Scientific, Health, Dental Vision, Retirement, Benefits, Remote, Senior Biostatistician.
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Job Description: The Senior Clinical Research Coordinator (CRC) is responsible for managing and overseeing the day-to-day operations of clinical trials, recruiting and screening study participants, as well as documenting and reporting on the daily operations of assigned trials.
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The Clinical Research Supervisor reports to the Research Administrator, Clinical Trials Manager, Research Vice Chairs and works directly with Principal Investigators within the Department of Obstetrics, Gynecology and Women's Health on the execution of reproductive health research studies, focusing on protocol development and coordination, supervising research/study assistants, and data cleaning and monitoring.
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Develop and nurture strategic partnerships within ASCO and in appropriate sectors of the health community to conduct ASCO research and support implementation of rigorous clinical cancer research methods and those that improve access to trials for patients with cancer.
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Experience reading and interpreting clinical trials research protocols. The Clinical Trials Office (CTO) at UCSD's Moores Cancer Center administers many clinical trials on behalf of its member investigators, including trials sponsored by National Cancer Institute cooperative groups, pharmaceutical companies, and physician investigators.
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Sarah Cannon Research Institute (SCRI) is one of the world’s leading oncology research organizations conducting community-based clinical trials. It has conducted more than 750 first-in-human clinical trials since its inception and contributed to pivotal research that has led to the majority of new cancer therapies approved by the FDA today.
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Bachelor’s degree, preferably in biological sciences, health care management, or life sciences research; BSN/RN or experience with management of clinical trials. Review and track essential regulatory documentation from clinical sites before study start-up and throughout study conduct.
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Assist with Otsuka's clinical trials program, including registrational, post-marketing and Investigator-Sponsored Trials (ISTs), health economic outcomes research, other specific medical collaborations; provide clinical expertise and feedback regarding operational management of clinical trials to ensure optimal site selection and performance.
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Position Overview : As a Remote Legal Assistant / Communications Specialist, you will be responsible for monitoring client communications, primarily through our chat system, and ensuring that information is quickly and accurately relayed to the appropriate team members for follow-up and execution.
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The Frederick National Laboratory is a Federally Funded Research and Development Center (FFRDC) sponsored by the National Cancer Institute (NCI) and operated by Leidos Biomedical Research, Inc. The lab addresses some of the most urgent and intractable problems in the biomedical sciences in cancer and AIDS, drug development and first-in-human clinical trials, applications of nanotechnology in medicine, and rapid response to emerging threats of infectious diseases.
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We are seeking a highly organized and detail-oriented Remote Legal Assistant / Communications Specialist to join our team and help us maintain seamless communication and operational efficiency.
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Company Overview : We are a fast-growing family law firm helping our clients stand up for themselves in Child Custody, Divorce, child welfare defense (DHR) and adoption cases. Flexible, fully remote work environment.
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Assist in drafting routine legal correspondence, document management, and basic legal research. Efficiently route client inquiries, updates, and tasks to the appropriate team members for timely follow-up.
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clinical research set up trials remote jobs Title: clinical
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