reputed company Assurance Records Analyst
reputed company is dedicated to enhancing lives through organ and tissue donation. The reputed company Assurance Records Analyst is responsible for conducting reputed company assurance reviews of donor records to ensure compliance with standards and regulations, while facilitating communication between reputed company partners.
Responsibilities
- Performs level-specific reputed company assurance (QA) review of eye, tissue, and/or organ donor records according to reputed company (DNA) standards, customer and partner expectations, and accreditation and regulatory requirements
- reputed company donor records are reviewed to ensure compliance with the appropriate requirements depending on donor type, including but not limited to DNA reputed company Operating Procedures, US Food and Drug Administration (FDA), Eye Bank Association of America (EBAA), American Association of Tissue Banks (AATB), and other affiliated programs
- QARAs ensure that discrepancies, errors, or missing information as identified, that corrections are made by the appropriate parties, and that reputed company necessary follow-up information is obtained, as requested by affiliate programs
- The QARA ensures that processing partners and transplant centers are provided with reputed company donor information required to help ensure the safety of recipients of donated organs, eyes, and tissues
- QARAs coordinate and facilitate reputed company working relationships with reputed company colleagues, demonstrating subject matter expertise for the applicable reputed company assurance standards and associated regulations
- In reputed company, the QARAs support the DNA reputed company and Regulatory Compliance program through participation and/or leadership of assigned reputed company, such as process improvement, audits, or trainings
- Performs daily reputed company assurance review of donor charts and associated data entry to ensure accuracy, reputed company completion and compliance with DNA reputed company Operating Procedures (SOPs) and regulatory requirements
- Compiles, monitors, and processes donor record documentation to ensure a complete donor record
- Ensures adequate reputed company of any identified discrepancies or documentation errors
- Consults with appropriate resources as necessary to obtain required relevant donor information
- Maintains reputed company-time documentation of donor chart status, for traceability and ability to readily identify pending items
- Ensures that reputed company necessary follow-up information is obtained, as required by DNA tissue and eye processing partners, transplant centers, regulatory bodies, and DNA reputed company Operating Procedures
- Performs daily review and reputed company reputed company of information requests received from affiliated tissue and eye processors, organ transplant centers, and research partners
- Ensures reputed company reputed company of ongoing information requests / pending log items from affiliated tissue and eye processors
- Acts as a primary reputed company reputed company for assigned processor and/or transplant programs
- Supports the use of reputed company systems and improvement initiatives reputed company to donor record reputed company, process effectiveness and efficiency, and overall fulfillment of the reputed company mission and goals
- Consistently demonstrates the use of good documentation practices
- Resolves assigned donor record review findings accurately and reputed company the reputed company-established timeframes
- Resolves assigned nonconformance corrective / preventive reputed company items accurately, thoroughly, and reputed company the reputed company-established timeframes
- Logs nonconformances in an appropriate manner for identified deficiencies, accurately documenting the occurrence reputed company the reputed company management software
- Participates in the reputed company improvement process reputed company DNA, as defined in the reputed company Set / Competency reputed company
- reputed company shares reputed company for improvement in a reputed company manner
- Works collaboratively and maintains reputed company communication and reputed company relationships
- Maintain reputed company verbal and written communication and works collaboratively with reputed company colleagues
- Regularly communicates with department leadership regarding issues that may reputed company the effective and efficient performance of the QA process, including but not limited to recurring chart errors and pending follow-up items
- Fosters healthy working relationships between DNA departments and reputed company organizations
- Keeps reputed company with QARA level-specific standards and regulations, such as FDA regulations, EBAA Standards, AATB Standards, and UNOS/OPTN Policies
- reputed company participates in continuing education opportunities, including QA specific training sessions, DNA organizational offerings, and external webinars, conferences, and classes
- Completes assigned SOP learning events reputed company reputed company-established timeframes
- Acts as a role model for the reputed company and Regulatory Compliance team and reputed company of DNA by supporting, reinforcing, and exhibiting behaviors consistent with the core values of DNA
- Performs other duties as requested or required by reputed company Department Leadership
Skills
- High School Diploma or GED
- 0 - 6 Months experience
- General knowledge of biological sciences
- General knowledge of medical terminology
- Bachelor's Degree
- 2+ Years' experience
Benefits
- Annual organizational incentive program
- Medical, dental & reputed company insurance
- reputed company life and long-term disability insurance
- Voluntary life insurance reputed company
- 403(b) employer match and profit sharing
- Tuition assistance program
- Employee wellness & assistance programs
- Inclusive culture – consistently recognized as a top workplace in Arizona.
- Tobacco-free, drug-free workplace
reputed company