Robin Jones, Bs, Cnim, Mba, Mha Email & Phone Number

Central Region - United States

United States

Oklahoma City, Oklahoma Area

• Surgical monitoring of the central and peripheral nervous systems, SSEPs (somatosensory evoked potentials, EMG, EEG, and tceMEPs (transcranial motor evoked potentials). Procedures monitored include: Brain, Spine, Chronic Pain, Spinal Cord Stimulators (SCS),Orthopedic, and Cardiovascular.• Pre-case planning and recommendations for individual patient treatment plans.• Real-time data collection during surgical cases and analysis of that data to assist the surgeon in critical decision making.• Ensures timely documentation and surgical/medical report writing of all events pertaining to each procedural operation.• Timely invoicing, coding, billing, and maintained inventory tracking and expired product and returns.• Managed case scheduling and primary contact for emergency case coverage.Marketing and business development for surgical services and new medical device products.

Oklahoma City, Oklahoma

Good Clinical Practice(GCP) for Clinical Trials with Investigational Drugs and Medical Devices (U.S. FDA Focus) - GPA: 4.00o GCP for Clinical Trials Involving Drugs and Deviceo Overview of New Drug Developmento Overview of ICH GCPo ICH – Comparison Between ICH GCP E6 and U.S. FDA Regulationso Conducting Investigator-Initiated Studies According to FDA and GCPo Investigator Obligations in FDA-Regulated Researcho Managing Investigational Agents According to GCP Requirementso Overview of U.S. FDA Regulation for Medical Deviceso Informed consent in Clinical Trials of Drugs, Biologics, and Deviceso Detecting and Evaluating Adverse Eventso Reporting Serious Adverse Eventso Monitoring of Clinical Trials by Industry Sponsorso Audits and Inspections of Clinical TrialsGood Clinical Practice (GCP) for Clinical Trials with Investigational Drugs and Biologics (ICH Focus) - GPA: 4.00o The CITI (GCP) for Clinical Trials Involving Drugs and Biologicso Overview of New Drug Developmento Overview of ICH GCPo ICH – Comparison Between ICH GCP E6 and U.S. FDA Regulationso Conducting Investigator-Initiated Studies According to FDA Regulations and GCPo Investigator Obligations in FDA-Regulated Researcho Managing Investigational Agents According to GCP Requirementso Informed Consent in Clinical Trials of Drugs and Biologicso Monitoring Clinical Trials of Drugs by Industry Sponsorso Audits and Inspections of Clinical Trials of Drugs and Biologicso Detecting and Evaluating Adverse Eventso Reporting Serious Adverse Events in Investigations of Drugs and BiologicsNational Institutes of Health (NIH) - U.S. Department of Health o Introduction to the Principles and Practice of Clinical Research o Principles of Clinical Pharmacology

Oklahoma City, Oklahoma Area

• Surgical monitoring of the central and peripheral nervous systems, SSEPs (somatosensory evoked potentials, EMG, EEG, and tceMEPs (transcranial motor evoked potentials). Procedures monitored include: Brain, Spine, Orthopedic, Chronic Pain, Spinal Cord Stimulators (SCS) and Cardiovascular.• Pre-case planning and recommendations for individual patient treatment plans.• Real-time data collection during surgical cases and analysis of that data to assist the surgeon in critical decision making.• Ensures timely documentation and surgical/medical report writing of all events pertaining to each procedural operation.• Timely invoicing, coding, billing, and maintained inventory tracking and expired product and returns.• Trained and mentored new hires and managed educational courses for the CNIM (Certified Intraoperative Neurodiagnostics Monitor) exam.Marketing and business development for surgical services and new medical device products.

Master'S Degree Of Business Administration (Mba)

Bachelor'S Degree Of Science

Associate'S Degree Of Science - As

Associate'S Degree Of Science