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Responsible for the oversight and coordination of clinical trials, management and database management. 10+ years of experience within Phase I-IV clinical trials and knowledge of medical field.
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Responsible for the collection and handling of blood specimens and related assessment of volunteer safety used in diagnosing and tracking illnesses, drug testing, clinical trials, or other health-related areas requiring a blood sample.
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General knowledge of the drug and vaccine development process or clinical trials is a plus. Familiarity with Good Clinical Practices and/or experience of working in an FDregulated environment is desirable.
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Topography Health is a first-of-its-kind, physician-focused clinical trials platform. Our mission is to accelerate clinical research by increasing the investigative capacity of every physician, creating a new world of medicine where patients have seamless access to advanced research.
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Work with us to transform the future of digital platforms of cancer clinical trials. You’ll work closely with clients to transform cancer clinical trails. action employer that empowers our people to fearlessly drive change – no matter their race, color, ethnicity, religion, sex (including pregnancy, childbirth, lactation, or related medical conditions), national origin, ancestry, age, marital status, sexual orientation, gender identity and expression, disability, veteran status, military or uniformed service member status, genetic information, or any other status protected by applicable federal, state, local, or international law.
$81,800 - $186,000 a yearFull-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Direct health care members in the execution of trials and resolution of logistical constraints and assures all aspects of Good Clinical Practice (GCP) and federal regulatory requirements are met or exceeded.
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Provide leadership and medical expertise in the planning and implementation of CVIsupported vaccine clinical trials and related activities (e.g., epidemiological studies, vaccine preparedness studies, effectiveness studies, post-marketing pharmacovigilance, development and training of key staff, etc.
Full-timeExpandApply NowActive JobUpdated 13 days ago - UpvoteDownvoteShare Job
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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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Job Description Description We are looking for an experienced client and project manager who will drive the end-to-end management, execution, and growth of a portfolio of client engagements within pharmaceutical partners, including in the clinical trials space.
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The Sr MSL role also includes developing creative and innovative tactics for addressing the specific needs of key customers; coordinate and manage regional investigator trials; represent real time voice of customer input related product development opportunities; conduct clinical presentations to payer organizations and patient advocacy groups.
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Clinical Trials experience. to oversee data management and analysis support for the clinical research activities conducted by the Walter Reed Army Institute of Research (WRAIR) Military HIV Research Program (MHRP), the Emerging Infectious Diseases Branch (EIDB), and other affiliated programs of our Client.
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The Research Data Coordinator 2 is responsible for data management for phase I, II, and III oncology clinical trials conducted in the Lombardi Comprehensive Cancer Center (LCCC). Support all aspects of clinical research data management for clinical trials conducted in the LCCC Clinical Research Management Office (CRMO), including collection of data from source documents and medical records and completion of case report forms per sponsor requirements.
ExpandApply NowActive JobUpdated 14 days ago - UpvoteDownvoteShare Job
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The qualified candidate will report to the Head of Clinical Data Science and is expected to have the following responsibilities:· Perform integrative analyses of multi-omics data from clinical trials and research cohorts, including genomics, transcriptomics, proteomics, and imaging, to identify biomarkers related to treatment mechanism and response, and potential therapeutic targets.
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General Summary of PositionMedStar Health Research Institute has a unique opportunity for a Director Clinical Research Operations to join our Cardiology research team on the campus of MedStar Washington Hospital Center in Washington, DC.Responsible for oversight and coordination of CRN clinical trials that are managed by the CRN CRO. Responsible for the oversight and coordination of chart review and follow-up activities in the data coordinating center.
Full-timeExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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The ideal candidate will have experience supporting and managing proposals in the federal health and human services as well as in medical staffing support services, health operations and logistics, clinical trials research services, public health/epidemiology research, healthcare case management, healthcare systems modernization, data sciences and analytics for healthcare, performance evaluation, strategic digital communications, artificial intelligence and learning, and cloud hosting services.
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clinical trials jobs in Washington, DC
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