- Bristol Myers Squibb (Cambridge, MA)
- …Business Development function + Partners with Worldwide Patient Safety physicians in the ongoing review of safety data + Serves as the (co-)leader of the ... all of the following attributes: + Able to synthesize internal and external data to produce a clinical strategy + Able to ensure that the clinical program… more
- Edwards Lifesciences (Kansas City, KS)
- …inspiring journey. **How you'll make an impact:** + Field monitoring of studies and data collection for clinical trials, assess all data documentation, ... your ideas and expertise can change a patient's life. We generate extensive clinical evidence to demonstrate the effectiveness and safety of our innovations and how… more
- Mount Sinai Health System (New York, NY)
- …coordination of timed or sequenced events (ie serial vitals) and the accurate capture of clinical data for the purposes of the study and patient monitoring. + ... and unanticipated events to institutional offices and committees (ie Data safety monitoring, institutional review board, etc.)...+ Participates in the collection, compilation, and analysis of clinical program activity data and reports on… more
- HCA Healthcare (Savannah, GA)
- …Ensures the integrity of the data submitted on Case Report Forms or other data collection tools by careful source document review ; monitors data for ... medical and research terminology Computer skills including use of clinical trial database, electronic data capture, and...personal growth, we encourage you to apply for our Clinical Research Nurse opening. We promptly review … more
- HCA Healthcare (Port Charlotte, FL)
- …Ensures the integrity of the data submitted on Case Report Forms or other data collection tools by careful source document review ; monitors data for ... and research terminology + Computer skills including use of clinical trial database, electronic data capture, and...personal growth, we encourage you to apply for our Clinical Research Nurse opening. We promptly review … more
- University of Michigan (Ann Arbor, MI)
- …+ Minimum 3 years of directly related experience in clinical research and clinical trials is necessary. (Please review SoCRA's Definition of a Clinical ... Clinical Research Coord Inter TERM-LIMITED **Early Site Maintenance**...Study Operations (GCPs) 5. Study and Site Management 6. Data Management and Informatics 7. Leadership and Professionalism 8.… more
- SSM Health (IL)
- …range as permitted by law. **Job Summary:** Performs concurrent analytical reviews of clinical and coding data to improving physician documentation for all ... **Worker Type:** Regular **Job Highlights:** Must have prior experience as a Clinical Documentation Specialist **Required Qualifications:** + 1 year of experience as… more
- Kelly Services (West Point, PA)
- …to SM for data management activities (eg, EDC, DRP, CRFs) + Monitors data issues requiring clinical input + Monitors central lab reports and other external ... **Senior Clinical Scientist I** **Therapeutic Areas: Oncology & Immunology**...including development of the Medical Monitoring Plan (MMP) and review of SAE reports + Sets up/supports SAC, DMC,… more
- University of Michigan (Ann Arbor, MI)
- …+ Minimum 2 years of directly related experience in clinical research and clinical trials is necessary. (Please review SoCRA'sDefinition of a Clinical ... Clinical Research Coord Assoc **Early Site Maintenance** We...Study Operations (GCPs) 5. Study and Site Management 6. Data Management and Informatics 7. Leadership and Professionalism 8.… more
- University of Michigan (Ann Arbor, MI)
- …+ Minimum 3 years of directly related experience in clinical research and clinical trials is necessary. (Please review SoCRA?s Definition of a Clinical ... Clinical Research Coord Inter **Early Site Maintenance** We...Study Operations (GCPs) 5. Study and Site Management 6. Data Management and Informatics 7. Leadership and Professionalism 8.… more