- Pixalate, Inc. (New York, NY)
- …in a cost-effective and legally-compliant manner. Experience analysing legislative and regulatory obligations for applicability, under US and international laws and ... of the material terms and conditions of subscription and data licensing agreements for software-as-a-service (SAAS) businesses, and significant experience… more
- Amgen (South San Francisco, CA)
- …Partner with Discovery Research, Clinical Pharmacology, Toxicology, Early Development, and Regulatory Affairs teams to ensure seamless progression from ... advance biomarker discovery. **Key Responsibilities Include:** + **Biomarker & Data Strategy:** Design and lead phase-appropriate biomarker strategies (pharmacodynamics,… more
- University of Pennsylvania (Philadelphia, PA)
- …for the Veterinary Clinical Investigations Center (VCIC) will complete documentation and data entry of patient visits and patient care for multiple trials and ... subjects for post-administration adverse events or reactions. + Prepare study data for statistical analysis. + Report research progress to Investigators, sponsors,… more
- University of Pennsylvania (Philadelphia, PA)
- …management of laboratory tools, documentation and processes to ensure regulatory compliance and timely completion of project/program deliverables. Job Description ... projects, harvesting tissue and performing flow cytometry, collecting and recording data , and providing lab organization assistance under the supervision of the… more
- Otsuka America Pharmaceutical Inc. (Boston, MA)
- …within a cross functional team (ie other RDAMs, brand marketing, market access, medical affairs and thought leader liaisons) necessary to meet business ... Rare Disease Selling Model creates a unified focus among account management, medical , patient access, market access and total office education to engage physicians… more
- Gilead Sciences, Inc. (Foster City, CA)
- …all therapeutic areas, around the world. In partnership with Clinical Research, Medical Affairs and Development Operations functions, ensures that all clinical ... are performed in accordance with all applicable SOPs, company policies and regulatory guidelines to provide timely delivery of high quality clinical data… more
- University of Utah (Salt Lake City, UT)
- …evening hours as needed to accomplish study objectives. **VP Area** Academic Affairs **Department** 00258 - Emergency Medical Physicians **Location** Campus ... FDA , NCI , NIH , NSF and/or other regulatory documents and research correspondence. 3. Coordinates participant study... Medical Record ( EMR ) to obtain medical /surgical history, lab values, and other relevant data… more
- Teleflex (Morrisville, NC)
- …in compliance with FDA's Quality System Regulation (QSR), ISO13485, the Canadian Medical Device Regulations, and all other international regulatory requirements ... :12676 **About Teleflex Incorporated** As a global provider of medical technologies, Teleflex is driven by our purpose to...2022-24 (5-17-22 FINAL), which is in part based on data provided by Symphony Health PatientSource(R) 2018-21, as is… more
- Fujifilm (Boston, MA)
- …with expense tracking and reporting (Salesforce.com) + Where appropriate, collaborate with the Medical Affairs Team. + Follow up to define pathway and respond ... what is working and not working. + Reviews sales data , assesses trends, and adjusts sales strategy based upon...all applicable US Food and Drug Administration (US FDA) medical device regulatory requirements, applicable ISO 13485… more
- City and County of San Francisco (San Francisco, CA)
- … Medical Services; and analysis of community public health data . Central administrative functions, including finance, human resources, information technology, and ... patient's medical record and departmental logs, in accordance with regulatory , hospital and departmental standards; identifies images and documents with patient,… more