- 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
- Sanofi Group (Morristown, NJ)
- …Life Cycle Management/marketed products. + Write nonclinical summaries for clinical Investigator Brochures, INDs, CTAs and NDAs/BLAs, Pediatric Investigation Plans, ... scientific perspective. + Ensure high scientific standards in conducting and reporting of nonclinical safety and investigative toxicology studies. Provide scientific… 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
- Johns Hopkins University (Baltimore, MD)
- Reporting to the Associate Administrator of Psychiatry and Behavioral Sciences, we are seeking an **_Assistant Administrator - Clinical_** who will manage and lead ... is responsible for financial planning, financial improvement initiatives, financial reporting , financial analysis, and fiscal planning. The role includes… 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 ... lives. Read more: careers.bms.com/working-with-us . **Job Title** Director, Early Clinical Development - Immunology **Functional Area Description** The Early … 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
- 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
- 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)
- …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 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
- Stony Brook University (Stony Brook, NY)
- …Sponsored Programs Associate II **Job Field** : Administrative & Professional ( non - Clinical ) **Primary Location** : US-NY-Stony Brook **Department/Hiring Area:** ... Contracts and Clinical Trials Officer **Required Qualifications (as evidenced by...degree (foreign equivalent or higher). Experience with federal and non -federal regulations and guidelines, cost principles, uniform administrative requirements… more