Generate reports on outstanding invoice payments for clinical study team review Review and ensure accuracy and completeness of clinical study files, enter into computerized tracking system, and file/scan for archive, for multiple clinical research trials Maintains current and active licensure and certification(s) to administer First Aid, BLS and CPR for emergent needs in healthy volunteer clinical research studies Support clinical research laboratory operations as needed Other incidental duties as assigned Required: >1–2 years of patient-facing experience in a clinical research, healthcare, or related medical setting. Clinical Operations Specialist 1 On Site Role Hours: Mon-Fri, 8am - 5pm Job Description: Identify, develop, recommend, and implement, moderately complex process development and process improvement solutions to optimize global trial workflow timelines, (e.g., device return aging issues, status of open device issues/queries, etc.) Develop and execute device processes associated with clinical trials.