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The center will function as a hub for microbiome data partnerships and a conduit for microbiome-based clinical trials. The CHOP Center for Microbial medicine will focus on developing microbiome-informed clinical diagnostics and microbiome-based therapeutics.
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Description Clinical Research Coordinator B ResponsibilitiesThis individual will work under general supervisionThe CRC will be responsible for the coordination of complex oncology clinical research protocols, including accurate data collection and overseeing the quality of the clinical trial data and records, scheduling and conducting study initiation and monitoring visits, and participating in ongoing study protocol training.
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The coordinator will oversee one or more clinical trials ensuring that the integrity of the protocol is maintained, all data and queries are answered in a timely manner, appropriate AEs and SAEs are reported to the sponsor and IRB per protocol.
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Prior experience in providing MSL-level support to products or devices in endocrinology and/or rare disease, including KOL development, investigator-initiated clinical trials, publications and educational programs, highly preferred.
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Hospital paid retirement plan and tax-sheltered annuity plan About the Termeer Center Seeking an experienced oncology RN for this 22-chair clinical trials research unit specializing in first-in-human, Phase 1 Clinical trials.
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Also work on FLOW that enables the connection between clinical trials and real-world data, expediting the generation of real-world evidence to ultimately improve patient outcome. We offer a comprehensive, yet flexible approach, based on the foundational elements of Identity, Privacy, Governance and Exchange (IPGE), that synchronizes unparalleled Identity management with built-in Privacy compliance and Governance, providing the ability to discover and Exchange a near limitless combination of data at a record pace.
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Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market.
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Ensure accurate data collection and management in accordance with Good Clinical Practice (GCP). Serve as the primary investigator for clinical trials, ensuring adherence to study protocols and regulatory requirements.
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The Statistical Analyst A will use standard SAS and/or STATA programming skills to create analytical datasets from clinical trials, surveys and health care claims, to construct and standardize outcome measures and other analytical variables through data cleaning and data manipulation, to provide descriptive and analytical reports, and to perform specialized statistical analyses.
$88,000 a yearFull-timeExpandApply NowActive JobUpdated 2 months ago - UpvoteDownvoteShare Job
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Experience with data collection, and development of data quality and outcome reports desirable;Experience with Medidata Rave required;Experience with an object-oriented programming language required, C# experience preferred;Bachelor's degree preferred;Familiarity with regulations governing clinical data (GCP, ICH);Familiarity with Operational Qualification/Performance Qualification and UAT (User Acceptance testing) execution and documentation.
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Under the direction and guidance of the principal investigator (PI), they will provide analytic support for research involving prospective data from clinical trials and observational studies, electronic health records, large administrative, claims, and echo imaging databases.
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Summary: The Clinical Research Nurse performs an essential role supporting the principal investigator in the conduct of clinical trials to ensure compliance with all aspects of the protocol and accuracy of data collection.
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Nurses within our unit are trained in delivery of chemotherapy and biotherapy, autologous stem cell transplant and clinical research trials. Assists with data collection for nursing history and physical (vital signs, height, weight, blood sugar results, functional status) and communicates changes to the RN or CRNP in a timely fashion.
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Coordinate Pharmaceutical Industry related activities within the Operations office, including collaborating with grants and contracts team, clinical operations team, protocol development team, lab science team, data management and statistical teams.
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Runs portions of clinical trials from startup to closeout, including protocol coordination (screening, recruiting, enrolling, consenting), feasibility planning, data management, biological specimen management, preparation for monitoring visits, and regulatory and/or IRB document preparation.
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clinical trials data jobs in Philadelphia, PA
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