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Reporting to the Vice President of Clinical Operations, the Trial Master File (TMF) Associate Director / Director serves a key role, working across the organization for the execution of TMF Operations processes and strategy.
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We are seeking a talented and experienced Clinical Trial Management Associate to work hybrid or remotely based in our South San Francisco office. The Clinical Trials Management Associate will work closely with Technical Operations to ensure drug product quality and delivery, Translational Sciences to ensure timely site biomarker sample collection and shipments, and support the clinical operations team with TMF filing and other duties as assigned.
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Trial Master File Records Specialist (TRS) Responsibilities. The TRS will provide services onsite (hybrid position) at our Ridgefield, CT location supporting our Trial Master File (TMF) team.
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As a Senior Trial Attorney, you’ll represent clients under both commercial and personal lines insurance policies independently as lead counsel, as well as be part of a larger team as needed. Requires minimal managerial oversight and guidance from the Managing Trial Attorney and NTD Leadership in all aspects of core duties and job responsibilities.
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Previous experience as a clinical research coordinator, clinical research associate, or related role is preferred. Activities may include providing assistance with establishing and maintaining trial regulatory files, coordinating FDA and IRB filings, establishing and maintaining electronic data systems to facilitate data capture and storage across multiple trial sites, site startup and closeout activities, maintaining trial participant records, and assisting with periodic internal site audits for multiple clinical trials.
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The investigator-initiated clinical trial management supervisor will work very closely with USC/Norris Cancer Center physician-scientists, various CISO services and teams, Data Science Shared Resource and other cancer center core services to ensure that IITs are of the highest quality.
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Responsible for managing relationships with CROs and other vendors for all study activities including study start-up, close out, and completion of Trial Master File. Previous experience as a Clinical Research Associate preferred, but not mandatory.
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As the Trial Visit Monitor - Mental Health Consultant (MHC), other duties will include:Referrals and MonitoringEvaluate referrals from local acute care hospitals, the state hospital, and other commitment sites.
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Plan, implement & ensure maintenance detailed integrated trial timelines from study outline though CSR (Gap: GCTM/CPL need a planner, e.g., MS Project, to show end to end project timelines and to build trust in organization.
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Reporting to the Associate Director of Clinical Operations, this individual will have primary responsibility for trial management within in vivo, regenerative medicine, or oncology indications.
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To qualify for this Trial Attorney (Core) position at the IC-13 level, you must possess two (2) years post J.D. legal experience, one of which was specialized experience equivalent to at least the IC-12 level in the Federal government, which has equipped you with the skills needed to successfully perform the duties of the position.
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The Division of Hematology-Oncology is seeking an experienced Senior Clinical Trial Specialist to join our team. Responsible for completing the administrative and operational tasks necessary to conduct Site Initiation Visits and Interim Monitoring Visits with clinical trial sponsor representatives; you will also serve as the primary administrative support to the Research Nurse Manager and Clinical Research Operations Manager.
$24.28 - $48.04 an hourExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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The Clinical Trial Manager Associate will report to the Senior Director, Clinical Operations and will be responsible for providing support to the clinical operations study teams for assigned responsibilities of a study/studies.
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The USC Norris Comprehensive Cancer Center’s Clinical Investigations Support Office (CISO) is seeking an Investigator-initiated Trial Management Supervisor to join its team. This person will also work closely with CISO Director and Associate Director in ensuring optimal support for IIT development and data management.
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Key responsibilities: This position will be part of a talented team that is responsible for the growth, ongoing maintenance and development of a large-scale server farm running primarily on Linux and UNIX. Provide Level 2 support for complex system and applications, rolling out new systems, maintaining, migrating, upgrading and improving the long-term performance of the systems.
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Title: trial associate Company: Leap Therapeutics
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