Overview
Quality Assurance Monitor 238468 Jobs in United States at Medix™
Title: Quality Assurance Monitor 238468
Company: Medix™
Location: United States
We are looking to add a Quality Assurance Clinical Trial Monitor to our growing team. This is a heavy travel role with someone expected to be on the road 50-60 percent of the time. Previous in Quality Assurance or Monitoring of phase 1-4 clinical trials is required.
Central Time Zone Preferred
The QA Clinical Trial Monitor will use judgment and experience to evaluate overall performance of site and site staff and to provide recommendations regarding site-specific actions following company outlined QA assessments; immediately communicates/escalates serious issues to the QA Director and develops action plans per the Quality Assurance Monitoring Plan to include by not limited to items detailed below.
Assesses site processes to facilitate execution of site-level activities and identify operational efficiencies and process improvements.
Provides guidance at the site and project level towards audit readiness standards and supports preparation for audit and required follow-up actions.
May provide training or guidance to site staff on execution of study related activities to follow company SOPs, local and federal regulations, and guidelines.
Applies actionable item(s) resolution techniques remotely and on site, and provides guidance to site staff as necessary, to drive actionable item resolution to closure within agreed timelines.
Utilizes available hardware and software to support the effective conduct of the clinical study data review and capture.
Verifies site compliance with electronic data capture requirements, ICH/GCP Guidelines and other applicable guidance, relevant regulations, and company SOPs/processes.
Facilitates preparation and conducts review of study specific items for sponsor audits and FDA inspections.
Documents QA Assessment activities via reports following QA Monitoring Plan to note and track all observations, ongoing status and assigned action items to resolution.
Conducts Source Document Review of appropriate site source documents and medical records to verify execution of critical study related activities, including obtaining informed consent, accurate and complete clinical data entry in the case report form (CRF) compared to site source documents and medical records.
Qualifications:
Bachelor’s degree or RN in a related field or equivalent combination of education, training, and experience.
Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements.
Must demonstrate good computer skills and be able to embrace new technologies.
Excellent communication, presentation, and interpersonal skills.
Ability to manage required travel of up to 50-70% on a regular basis.
