Senior Auditor Clinical Affairs

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 115,000 colleagues serve people in more than 160 countries. Working at Abbott At Abbott, you can do work that matters, grow, and learn, care for yourself and your family, be your true self, and live a full life. You’ll also have access to: Career development with an international company where you can grow the career you dream of. Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year. An excellent retirement savings plan with a high employer contribution. Tuition reimbursement, the Freedom 2 Save student debt program, and FreeU education benefit - an affordable and convenient path to getting a bachelor’s degree. A company recognized as a great place to work in dozens of countries worldwide and named one of the most admired companies in the world by Fortune. A company that is recognized as one of the best big companies to work for as well as the best place to work for diversity, working mothers, female executives, and scientists. The Opportunity The position of Senior Auditor provides auditing and Quality Assurance activities in order to assure that the systems, processes and performance of internal and external clinical study sites comply with applicable laws, regulations, Standard Operating Procedures, protocols and guidelines and meet Sponsor requirements. Independently conduct or take lead role with multiple auditors, plan and conduct external clinical study audits, internal specimen collection audits, clinical data verifications and master file audits. As SME, mentor/coach/train other internal QA auditing staff, manage contract auditors as well as support internal investigator training sessions. Train and manage other personnel/process to perform data audits to meet submission timelines to Regulatory agencies. Main Responsibilities Maintains current knowledge of applicable FDA regulations, ICH GCP, FDA regulations and other applicable regulatory standards to maintain effectiveness as a Clinical Affairs Auditor. Conducts audits independently and act as lead when multiple auditors present. Prepares and maintains a Division audit schedule for GCP activities, reviews and agrees to site audit schedules, plans, observations and ratings. Monitors and analyzes both internal and external audit outcomes and reacts/directs/manage as appropriate. Participates in site-led audits of the site’s quality system, called upon as an SME during CRQS audits/regulatory inspections as well as performs activities such as scribe and/or document reviewer. Prepares reports to Senior Management documenting audit activities, metrics, findings and resolutions and raises significant issues of noncompliance. Manages post-audit activities and follows up on any necessary corrective and preventive actions and resolves any conflicts. Manages and maintains files and documentation associated with all audit activities. Identifies and corrects GCP compliance deficiencies along with successful facilitation of an external inspection/audit that could avoid suspension of new product approvals through significant regulatory actions. If not prevented, the action can result in loss of business opportunities and can negatively impact the profitability of the company. Has a thorough knowledge of Good Clinical Practice (GCP), ICH and FDA regulations and guidelines and must be able to interpret, explain and apply. Possesses a proven understanding of clinical processes and systems and experience with medical device clinical trials and substantial experience with GCP audits. Has excellent organizational, interpersonal and communication skills both orally and in writing. Is an experienced PC user proficient with Microsoft Word, Excel and PowerPoint. Proficient in auditing databases, trial master files, investigator sites, statistical/clinical study reports, process/systems, for cause audits. Can evaluate complex systems and determine the level of compliance to regulations and standards. Serves as liaison to all appropriate Division departments/teams to ensure expeditious compilation of projects and corrective action for audit observations. Assists in development of training materials, manages SOPs and process improvement activities. Has willingness to travel. Required Qualifications Education: Bachelor’s Degree in biology, chemistry, microbiology, or related life sciences. 6–8 years in Quality Assurance or clinical research. 3–4 years in QA/GCP auditing. Experience with paper-based data management systems as well as EDC data management systems. Ability to investigate and analyze information and draw conclusions. Requires knowledge and training in CAPA. Detail oriented, accurate and able to independently determine and develop approach to solutions. Preferred Qualifications Certification (ASQ CQA or Lead Auditor). An equal opportunity employer, Abbott welcomes and encourages diversity in our workforce. We provide reasonable accommodation to qualified individuals with disabilities. The base pay for this position is $99,300.00 – $198,700.00. In specific locations, the pay range may vary from the range posted. #J-18808-Ljbffr Abbott Laboratories