- Olympus Corporation of the Americas (Center Valley, PA)
- …associated follow-up activities (eg, reports, corrective actions). + Perform reviews of clinical study documentation for data integrity and compliance with GCP ... guidelines and regulation, including Quality Control checks of the eTMF to ensure it is...development, and outside vendors where applicable. + Experience auditing clinical vendors, Clinical Research Organizations ( CRO… more
- Otsuka America Pharmaceutical Inc. (San Juan, PR)
- …to add value strategically. + Provides strategic oversight in our vendor and CRO relationships and provides clinical input into their governance committees. + ... + Working knowledge of associated disciplines, including immunology, biostatistics, clinical pharmacology, formulation science, data management, and medical… more
- Otsuka America Pharmaceutical Inc. (Annapolis, MD)
- …innovations to add value. + Provide strategic oversight in our vendor and CRO relationships and provide clinical input into their governance committees. + ... + Working knowledge of associated disciplines, including immunology, biostatistics, clinical pharmacology, formulation science, data management, and medical… more
- J&J Family of Companies (Spring House, PA)
- …and leads in Data Management and Central Monitoring, Programming Leads, Clinical Data Standards, Regulatory Medical Writing Leads, and system support ... would be preferred. + Advanced knowledge of programming and industry standard data structures, thorough understanding of end-to-end clinical trial process and… more
- US Tech Solutions (Cambridge, MA)
- …the specific clinical study budget trackers + Review invoices against ** CRO /Vendor contracts and study progress** to provide recommendation of approval or not to ... Act (US)** + Responsible for data entry and status updates within the Ipsen Clinical Trial Management System (CTMS) + When assigned on a study, get access to the… more
- IQVIA (Durham, NC)
- …research programs including review of new business proposals, preclinical and/or clinical data , study protocols, training materials, informed consent, ... study proposals, preparation of training sessions, and interpretation of clinical data , report writing, etc. . Assists... research as study physician/investigator or in the Pharma, CRO , or Biotech industry . Ability to work in… more
- Kelly Services (St. Louis, MO)
- …experience. + **Prior experience working in a laboratory setting or with scientific/ clinical data .** + Strong attention to detail and excellent organizational ... data quality and compliance with standards. + Assist clinical and regulatory teams with data review,...implement data reporting specifications and resolve any data -related queries from clients. + **Support quality control… more
- Bristol Myers Squibb (Albany, NY)
- …Payment) + Provide scientific support at promotional meetings by presenting scientific and clinical data , by evaluating speakers and by giving support to ... personnel to any identified Adverse Events + Actively support CRO sponsored studies as agreed with home office medical...act as a team player + Translating scientific or clinical data into an understandable and valuable… more
- University of Florida (Gainesville, FL)
- …portfolio of human clinical trials. + Interpreting and collecting medical and clinical data for prospective and existing enrolled subjects on assigned ... portfolio of human clinical trials. + Interpreting and collecting medical and clinical data for prospective and existing enrolled subjects on assigned … more
- J&J Family of Companies (Santa Clara, CA)
- …of clinical study documents. This may also include management of Clinical Events Committee(s) and Data Safety Monitoring Board(s). **Essential Job ... escalating vendor management issues as appropriate + Management of Clinical Events Committees (CEC) and Data and...sites, as needed + Liaison for safety-related questions from Clinical Affairs, CRO , monitors, Field Clinical… more