- 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
- Beth Israel Lahey Health (Burlington, MA)
- …**Time Type:** Full time **Work Shift:** Day (United States of America) **FLSA Status:** Non -Exempt **When you join the growing BILH team, you're not just taking a ... job, you're making a difference in people's lives.** The Clinical Research Coordinator will be responsible for the coordination and administration of multiple… 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
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