- System One (Poquonock Bridge, CT)
- Job Title: Non - clinical reporting and submission scientist Location: Groton, CT - Hybrid Hours/Schedule: Monday - Friday / First shift / Hybrid once ... 3 days onsite Primary Responsibilities + Prepare PDM reports in an electronic submission ready format required for submission level documents such as… more
- Takeda Pharmaceuticals (Boston, MA)
- …monitoring reports. + Lead and organize Trial Reporting activities for assigned clinical studies and non - clinical data cleaning activities. + Developing ... empower you to shine? Join us as the Director, Clinical Trial Reporting based remotely reporting...submission compliance. + Ensure that technologies used in clinical trial(s) (eg, Jreview, Veeva CDM, R, RShiny) at… more
- University of Pennsylvania (Philadelphia, PA)
- …IRB, including submissions, continuing reviews, amendments, modifications, and adverse event reporting . Clinical Research Coordinator will assist with creation ... IRB, including submissions, continuing reviews, amendments, modifications, and adverse event reporting . Clinical Research Coordinator will assist with creation… more
- University of Pennsylvania (Philadelphia, PA)
- …role and responsibilities including the limitations of the role in performing clinical study activities. Understand reporting structure and who to contact ... additional or supporting documentation including local laboratory or imaging reports and clinical encounter notes. Assist with reporting and record data… more
- Johns Hopkins University (Baltimore, MD)
- …Director and executive leadership team. The position is responsible for the non -faculty administrative staff in executing the Department's clinical , academic and ... the strategic development, operations, and continuous performance improvement of a clinical , academic, and research department. The Sr. Administrator has a matrix… more
- Georgetown Univerisity (Washington, DC)
- …research. + Oversee regulatory maintenance, adherence with ongoing training requirements, accurate reporting of clinical trial visits via the OnCore/CTMS system, ... organizations in the region strengthen our work and expand its reach. The Clinical Research Coordinator (CRC) is responsible for managing and coordinating 4-7 out of… more
- University of Rochester (Rochester, NY)
- …and update Research Base trials on ClinicalTrials.gov. + Ensure accuracy in post- submission Human Subjects reporting for the NCORP grant, resolving discrepancies ... individual, and internal equity considerations._ **Responsibilities:** GENERAL PURPOSE: The Sr. Clinical Trials Project Mgr. role supports the URCC NCORP Research… more
- Johns Hopkins University (Baltimore, MD)
- We are seeking an **_Associate Administrator - Clinical ._** With a matrixed reporting relationship to the Director of the Divisions of Geriatric Medicine and the ... management) at Bayview Medical Center. + Provide, review, and analyze the clinical practice finances of the division. Develop appropriate billing strategies to… more
- Bristol Myers Squibb (Cambridge, MA)
- …regulatory reports, briefing books and submission documents to support closure, clinical narratives, reporting and filling of the study in partnership with ... and in their personal lives. Read more: careers.bms.com/working-with-us . **Director, Early Clinical Development (MD) - Hematology & Cell Therapy with Focus in… more
- Loyola University Chicago (Chicago, IL)
- Clinical Research Coordinator II Thank you for your interest in Loyola University Chicago. To view open positions, please enter your search criteria below. You may ... Preview | Apply for this Job Position Details Position Details Job Title CLINICAL RESEARCH COORDINATOR II Position Number 8150021 Job Category University Staff Job… more
- University of Texas Rio Grande Valley (Harlingen, TX)
- …Medicine/ Revenue Cycle FTE1.0 FLSAExempt Scope of Job To promote appropriate clinical documentation through collaboration with the School of Medicine clinical ... process is followed. Description of Duties * Obtains and promotes appropriate clinical documentation through interaction with clinical staff and physicians to… more
- University of Colorado (Aurora, CO)
- …with other Administrators in the grant/contract process including development, submission , receipt, and reporting . Must have excellent organizational, ... ** Clinical Science Program Manager** **Description** **University of Colorado...in program/project budget development processes, including grant writing and submission processes, and regularly reviews to ensure alignment. +… more
- University of Virginia (Charlottesville, VA)
- …meetings. Payer & Accreditation Reporting * Support payer clinical data submission requirements including outcomes tracking, intervention documentation, ... clinical initiatives such as disease management, payer-driven outcomes reporting , accreditation compliance, and operational standardization across specialty pharmacy… more
- Houston Methodist (Houston, TX)
- At Houston Methodist, the Director Governmental Reporting is responsible for ensuring that Houston Methodist meets all internal and external financial and ... governmental reporting requirements. Requirements include Medicare cost reports, Federal Tax Returns Health and Human Services (HHS)/Centers for Medicare and… more
- Charles River Laboratories (Shrewsbury, MA)
- … kits and materials for clinical studies ⦁ Receive and accession clinical and non - clinical regulated study samples following Good Laboratory Practices ... with clients and/or sample management group and/or senior scientific staff to address/resolve clinical and non - clinical regulated study sample and manifest… more
- Gilead Sciences, Inc. (Santa Monica, CA)
- … clinical development: + Accountable for the design, conduct, evaluation, close-out and reporting of clinical trials across the solid tumor portfolio. + Lead ... study or investigator documentation, contributions to data analysis plans, study reporting , and clinical development inputs into regulatory documentation,… more
- University of Pennsylvania (Philadelphia, PA)
- …shortened during periods of data lock or in preparation for abstract/manuscript submission . Responsible for IND/IDE reporting and/or assisting Sponsor with ... programs and resources, and much more. Posted Job Title Clinical Research Coordinator A Job Profile Title Clinical...all tests and assessments at each visit are performed, reporting adverse events and ensuring review and appropriate follow-up… more
- University of Pennsylvania (Philadelphia, PA)
- …be shortened during periods of data lock or in preparation for abstract/manuscript submission . Responsible for IND reporting and/or assisting Sponsor with annual ... health and wellness programs and resources, and much more. Posted Job Title Clinical Research Coordinator B/C (Abramson Cancer Center) Job Profile Title Clinical … more
- University of Rochester (Rochester, NY)
- …of the individual, and internal equity considerations._ **Responsibilities:** The Clinical Division Administrator, Otolaryngology division will develop the business ... the URMC network). **SCHEDULE:** 8 AM-5 PM **GENERAL PURPOSE:** The Clinical Division Administrator, Otolaryngology division will develop the business management… more
- University of Pennsylvania (Philadelphia, PA)
- …and other treatment agents or study interventions, as appropriate. + Review all clinical and laboratory data and adverse events, reporting in real-time to ... of health and wellness programs and resources, and much more. Posted Job Title Clinical Research Nurse C/D (Abramson Cancer Center) Job Profile Title Clinical … more