- Abbott (Sylmar, CA)
- …experience + Minimum 7 years of progressively more responsible work experience in medical device industry or equivalent + Demonstrated ability to apply ... + Demonstrated experience in authoring or co-authoring peer-reviewed scientific publications + Medical device experience in the cardiac space preferred Apply Now… more
- Abbott (St. Paul, MN)
- …including Clinical Medicine, Engineering, Marketing and Regulatory Affairs required. Medical device industry experience preferred. Training and experience in ... and get on with their lives. As the Sr. Clinical Engineer, you'll be part of our Electrophysiology (EP)...or, Design Validation and GLP study experience in the medical device industry. + Demonstrated ability to… more
- Terumo Neuro (Aliso Viejo, CA)
- …committees as well as reports of committee findings and results. + Partner with clinical research project managers and Medical Affairs and Safety Manager ... clinical safety support to regulated clinical device studies or relevant clinical research...of adverse events. 5. Class III medical device safety experience. **External-Facing Title:** Specialist, Clinical … more
- IQVIA (Carlsbad, CA)
- …stage of their well-being journey. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life ... and welfare and/or other benefits. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life… more
- Teleflex (PA)
- …against contracts. * Clinical contract work experience from pharmaceutical, medical device , healthcare, or Contract Research Organizations (preferred). ... requirements (eg, CFR, GCP) and documents. * Moderate knowledge of the clinical research process, medical terminology and healthcare compliance and privacy… more
- Danaher Corporation (Minneapolis, MN)
- …+ Bachelor's degree with 6+ years clinical quality experience within diagnostics or medical device industry, or Master's or Doctoral degree with 4 years of ... understanding of ISO 14155, 13485, 14971, 20916, in vitro diagnostic regulation (IVDR), medical device regulation (MDR), and pertinent sections of 21 CFR. +… more
- University of Rochester (Rochester, NY)
- …Regular Time Type: Full time Scheduled Weekly Hours: 40 Department: 400301 Emergency Research Admin Work Shift: UR - Day (United States of America) Range: UR ... GENERAL PURPOSE: Coordinates the activities associated with human subject research . **ESSENTIAL FUNCTIONS** + Coordinates the administrative details required to… more
- Edwards Lifesciences (Baltimore, MD)
- …Degree or equivalent in Nursing or related field, 5 years experience previous related medical device , Cathlab, and/or clinical experience in an acute care ... us and be part of our inspiring journey. The Clinical Specialist at IHFM plays a vital support role,...it relates to the business + Moderate understanding of medical device regulatory requirements and documents, … more
- Sanofi Group (Morristown, NJ)
- …biomarker (DBM) implementation in Sanofi trials. This position leverages your extensive clinical expertise, scientific acumen, and research experience to advance ... with the broader DBM team and stakeholders to develop research hypotheses grounded in clinical relevance, then...with 8-10 years of experience in life sciences, healthcare, medical devices, pharma or a related field + Strong… more
- MD Anderson Cancer Center (Houston, TX)
- …Engineering SME on various institutional initiatives including but not limited to, Medical Device Governance with emphasis on Cybersecurity measures, SCORE ... The primary purpose of a Clinical Engineer is to provide technical expertise and...(Huron Group) program, FDA GRC / Info-Sec Medical Device Classification and continuous efforts to… more