In this position, the QA Specialist will support the ProTrials Quality Assurance department. The QA Specialist will maintain the ProTrials’ Controlled Document System and ProTrials Training Program, and other QA supportive Good Clinical Practice (GCP) activities per ProTrials procedures and applicable regulatory requirements (FDA, ICH, etc.). The QA Specialist will participate during Sponsor audits and/or regulatory inspections, as required. Responsible for assessing, evaluating, and reviewing corporate operations against GCP regulations to assure real-time observation of activities, issue identification/resolution, including proper and timely documentation Facilitates and conducts internal and external audits and provides metrics and analysis of trends based on audit findings Assist in the conduct or arrangement of GCP training for all staff Maintain the Controlled Document and Training systems and oversee administrative support utilized in maintaining systems Manage process and tracks controlled documents from the Document Change Control Form (DCRF) process until document approval or retirement, including updating related Controlled Document, training logs, and trackers Responsible for providing quality oversight to the revision, review, and approval of controlled documents Work with document reviewers to advise and revise controlled documents as appropriate and ensure reviews are performed in a timely manner Responsible for providing input and support as appropriate to the creation of new controlled documents Works with QA Management and other departments to identify gaps in controlled documents and recommends solutions Communicate effectively with staff and management across departments on status of Controlled Documents and corporate training Participate in inspection readiness activities and corporate audits, sponsor audits and/or regulatory inspections, as required Works closely with others to determine root cause and potential preventive/corrective actions in support of the corporate CAPA Program. Identifies, classifies, and reports deviations, as appropriate, and typically works on more complex minor and/or major deviations. Ensure support for the timely closure of investigations Assist QA management with the evaluation of learning management systems and other QA technology, as required Assist in the preparation of quality metrics and reports Assist QA management team with other Clinical QA activities as required Other duties, as assigned

Lowry, a ReSource Pro company, is seeking a Senior Premium Audit Reviewer to execute complex audit reviews, support auditor development, and maintain quality oversight for high-priority accounts and test audit programs. This role provides mentoring during onboarding, supports file quality initiatives, and identifies trends that influence performance improvement. The Senior Premium Audit Reviewer is a key resource for both peer reviewers and leadership, ensuring accuracy and adherence to guidelines across auditing practices. Perform audit reviews across all audit types, focusing on oldest audits in the queue; provide coverage for reviewers. Conduct secondary reviews for paid review accounts; perform higher-level audit reviews requiring advanced quality assurance expertise. Monitor audit queues and assist in resolving audit bottlenecks. Review self-review audits submitted directly to billing to ensure they meet self-review eligibility and quality requirements. Monitor audit reports to detect trends or recurring issues. Track carrier return data and recommend process improvements. Collaborate with leadership on quality monitoring strategies and data analysis. Pull and analyze audit files to identify performance strengths and gaps. Share review results with leadership for delivery to the auditor who completed the original audit. Conduct reviews of test audits for designated carriers within the test audit program. Support onboarding of new reviewers by providing shadowing opportunities and ongoing mentorship via chat. Fill in on live learning platforms such as Zoom or Learning Academy, as well as any other area within the team, to support team initiatives. Support a positive workplace culture by promoting open, solution-oriented communication, encouraging teamwork, and maintaining a focus on shared goals and productivity.

• Responsible for assessing, evaluating, and reviewing corporate operations against GCP regulations to assure real-time observation of activities, issue identification/ resolution, including proper and timely documentation • Facilitates and conducts internal and external audits and provides metrics and analysisof trends based on audit findings • Assist in the conduct or arrangement of GCP training for all staff • Maintain the Controlled Document and Training systems and oversee administrative support utilized in maintaining systems • Manage process and tracks controlled documents from the Document Change Control Form (DCRF) process until document approval or retirement, including updating related Controlled Document, training logs, and trackers • Responsible for providing quality oversight to the revision, review, and approval of controlled documents • Work with document reviewers to advise and revise controlled documents as appropriate and ensure reviews are performed in a timely manner • Responsible for providing input and support as appropriate to the creation of new controlled documents • Works with QA Management and other departments to identify gaps in controlled documents and recommends solutions • Communicate effectively with staff and management across departments on status of Controlled Documents and corporate training • Participate in inspection readiness activities and corporate audits, sponsor audits and/or regulatory inspections, as required • Works closely with others to determine root cause and potential preventive/corrective actions in support of the corporate CAPA Program. Identifies, classifies, and reports deviations, as appropriate, and typically works on more complex minor and/or major deviations. Ensure support for the timely closure of investigations • Assist QA management with the evaluation of learning management systems and other QA technology, as required • Assist in the preparation of quality metrics and reports • Assist QA management team with other Clinical QA activities as required • Other duties, as assigned

• "Deep diving" into our products, technology and profession • Analyzing software requirements • Manually testing one or several Veeam products • Communicating with other participants of the product development process • Evaluating test results, maintaining defects database