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Reporting Relationships Reports to the Director, Accreditation, Cancer Registry and Clinical Research Qualifications Bachelor’s degree required. Responsible for the day to day operations of the Cancer Registry and administrative activities with regard to Quality Assurance, Regulatory and Database Management, Cancer Committee meetings, Tumor Board, and Breast Conference.
Full-timeExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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CommunicationIndependently/collaboratively performs responsibilities of Level I.Collaborate closely with study coordinator on patient updates and clinical issues to ensure prompt, accurate reporting to sponsor or other entities is handled within protocol/ regulatory guidelines.
$72,940 - $100,380Full-timeExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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Our team of 32,000 includes physicians, nurses, residents, fellows, and many other clinical and non-clinical associates working in a variety of settings across our health system, including 10 hospitals and more than 300 community-based locations, the largest home health provider in the region, and highly respected institutes dedicated to research and innovation.
Full-timeExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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As the medical education and clinical partner of Georgetown University for more than 20 years, MedStar Health is dedicated not only to teaching the next generation of doctors, but also to the continuing education, professional development, and personal fulfillment of our whole team.
Full-timeExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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Become well versed in regulatory and legal requirements applied to human research ethics, institutional research governance as well as operational compliance in the increasing complex clinical research sector.
ExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Your expertise as a Clinical Research Associate, coupled with your strong grasp of clinical research study protocols and your adeptness at integrating and adhering to Good Clinical Practice (GCP) and regulatory standards, constitute essential skills that will drive success in this role.
ExpandApply NowActive JobUpdated 10 days ago - UpvoteDownvoteShare Job
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We provide the depth of expertise necessary to advance programs, by providing a range of life science services including business development, program management, CMC, non-clinical, quality, regulatory, and strategic consulting with proven experience in biodefense/pandemic response and strategic product development.
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6 months of full- or collective part-time experience in Mohs surgery histopathology within the last three years under the supervision of a Mohs micrographic surgeon or 1 year of recent histology clinical or research laboratory experience.
Part-timeExpandApply NowActive JobUpdated 3 months ago - UpvoteDownvoteShare Job
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Previous practical experience in skin care or cosmeceuticals clinical research project, GCP qualification is an advantage. Closely collaborate with colleagues from research, development & innovation, applied innovation, product management , regulatory teams, marketing and sales, business development and contract management to ensure the success of the projects.
ExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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Oversees the Company’s current and future product and service offerings to support Cell Therapy research and development, as well as clinical manufacturing and bioprocessing. Demonstrated expertise in Cell Therapy development, manufacturing, tools, platforms and regulatory landscape.
Full-timeExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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We are seeking a Sr. Research Nurse that will report to the Principal Investigator(s), Research Nurse Manager, and Lead Research Nurse this position is responsible for the coordination and implementation of assigned clinical trials within the Genitourinary Disease Group.
$74,400 - $130,400 a yearFull-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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In addition to operational management of multiple research studies, the Senior Research Coordinator will see patients participating in ongoing clinical trials, and will be responsible for specimen collection, processing, and DOT/ IATA compliant handling and shipment.
Full-timeExpandApply NowActive JobUpdated 10 days ago - UpvoteDownvoteShare Job
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Obtains regulatory documentation for successful implementation, monitoring and evaluation of clinical trials. - Excellent knowledge of FDA and OUS regulations, GCP, ICH guidelines applicable to the conduct of clinical research.
ExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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This is a great role for anyone that aspires to be an enrollment specialist, clinical research coordinator, or eventually manager. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.
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Experience: 5 years Clinical experience within the field of Medical Surgical, Mental Health, Durable Medical Equipment, and/or Utilization Management, including significant experience in research methodology and systematic evaluation of medical literature and translation of evidence into policy in a healthcare setting.
$69,768 - $138,567 a yearRemoteExpandApply NowActive JobUpdated 2 days ago
clinical research regulatory jobs in Baltimore, MD
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