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The ideal candidate will have experience/expertise in the development, execution, and management of data collection and data quality review for clinical/health outcomes research studies, clinical trials, and/or digital health research studies.
$80 - $90 an hourFull-timeExpandApply NowActive JobUpdated 9 days ago - UpvoteDownvoteShare Job
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Manage and maintain vendor budgets for assigned clinical trials and process flows and data exchanges with global pharmacovigilance for clinical trial serious adverse events.
RemoteExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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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.
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The role oversees and manages the Development QA team and interacts cross-functionally with functional teams who interact with and/or support Preclinical and Clinical Trials, which include Preclinical and Clinical Operations; and, Product Development, GMP teams, Pharmacovigilance, Medical Writing, Biostatistics and Data Management to ensures compliance to the Quality Management System (QMS) and all applicable regulatory requirements.
Full-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Responsible for all clinical data management activities in clinical trials in accordance with Ferring SOPs and current regulatory requirements. Support and maintains clinical data management processes and data capturing systems for clinical trials by following Ferring SOP.
ExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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Extensive knowledge of broad array of systems including Clinical Trials Management System (CTMS); Risk Based Monitoring (RBM); Electronic Trial Master File (eTMF); Electronic Data Capture (EDC); Clinical Studies Operational Data Warehouse & Analytics; Site Training and Resource Management etc.
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Under supervision of the Clinical Research Manager of the Clinical Trials Unit, the Clinical Research Coordinator supports the clinical research efforts of the Cancer Center by providing comprehensive coordination and data management of multiple Phase I-IV cancer-related protocols according to Good Clinical Practices (GCP), internal standard operating procedure (SOPs), and University policies and procedures.
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The OHSU Knight Cancer Institute Clinical Research Coordinator is responsible for implementation and overall management of oncology clinical trials. The Knight Prostate Cancer Research Program has two openings for Clinical Research Coordinators (TI Sr. Clinical Research Assistants) working on complex therapeutic interventional clinical research protocols and data management.
Full-timeExpandApply NowActive JobUpdated 23 days ago - UpvoteDownvoteShare Job
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Looking for candidates with strong understanding of clinical trials, clinical specimen handling, vendor management, sample tracking / management experience, with strong Excel (VLookup) and LIMS experience.
ExpandApply NowActive JobUpdated 17 days ago - UpvoteDownvoteShare Job
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Bachelor’s degree in a health related field and 1 year of experience with clinical trials; previous experience with data management, or in a health care facility preferred.
$17.24 - $27.59 an hourFull-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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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.
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Experience with CDISC (SDTM); data collection requirements in oncology trials; and clinical data standards development and maintenance. Bachelor's degree in science or related area 10+ years of significant Standards Experience and/or Clinical Data Management (CDM) experience in biotech/pharma industry, hands-on experience in all aspects of data activities.
ExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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Remains current about new developments in Biostatistics and utilizes learnings to contribute to strategic initiatives in Statistics and Clinical Data Management. Experience in Phase I, II and III pharmaceutical clinical trials, preferably in trials whose data was submitted as part of an investigational new drug (IND) or new drug application (NDA) to the FDA.
ExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Specializes in the clinical domain and works across biostatistics, clinical trials/research, data management, health economics/RWE, medical affairs, statistical programming, and other R&D areas within pharma and biotech.
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The Statistical Analyst A will use standard SAS and/or Stata to create analytic datasets from clinical trials, health care claims, electronic medical records, and surveys; to construct and standardize analytical variables through data integration and data manipulation; to provide descriptive and analytic reports; and to perform statistical analyses.
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clinical trials data management jobs
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