Lab Data Entry QC Review - Mon-Fri, 10:00pm-6:30am

Eurofins USA Clinical Diagnostics•Lenexa, KS

1d•Onsite

About The Position

Eurofins Viracor LLC is seeking a Laboratory Data Entry QC Review associate responsible for the review and audit of order entry information and performing duties with a high degree of proficiency. This role also involves duties related to accessioning and data entry. Eurofins Viracor LLC is an equal opportunity employer and encourages individuals from all backgrounds to apply. Successful candidates will be required to pass a standard drug screen and a thorough background check as part of the pre-employment process. Eurofins Viracor LLC does not sponsor employment visas.

Requirements

High School diploma or equivalent required
Specimen processing experience preferred.
Must be comfortable with raw specimen handling.
Ability to read, interpret, and comply with documents such as internal SOPs, operating and maintenance instructions, and company policies.
Position may require evening and weekend hours.
Goal oriented, with excellent time management and organizational skills
Excellent interpersonal skills, with ability to interact effectively and work efficiently with people at all levels in an organization.
Excellent verbal & written communication skills
Keenly attentive to detail
Ability to keep sensitive information confidential.
High level of proficiency with PC-based software programs; strong database skills; 1 year of data entry experience preferred.
Minimum of 2 years of clinical laboratory experience or 1 year as a Level I
Demonstrate superior understanding of laboratory operations and department processes.
Advanced problem-solving skills
Minimum of 3 years of clinical laboratory experience or 1 year as a Level II
Demonstrate ability to manage workflow.
Higher level understanding
Demonstrated leadership abilities.
Demonstrated effective training skills.
Ability to direct other Associates as required.
Ability to assist Management in providing overall direction of workflow for Support Services as needed.
Ability to ensure applicable SOPs are being utilized and followed appropriately.

Nice To Haves

Specimen processing experience preferred.

Responsibilities

Demonstrate data entry proficiency with the Laboratory Information Management System (LIMS) and/or other test ordering systems.
Ability to prioritize and organize efficient workflow, demonstrating excellent time management skills.
Ability to maintain detailed and accurate records with great attention to detail, according to good documentation practices.
Make appropriate internal or external contact to resolve patient demographic issues or discrepancies.
Complete correction requests as needed in a timely manner.
Adhere to all Data Management policies and protocols.
Prepare completed records for long term/offsite storage as needed.
Examine samples for accuracy and other requirements (sample type, stability, volume, etc.)
Label samples for delivery to proper area(s)
Use and maintain applicable sample storage materials (i.e., dry ice)
Maintain quality control and quality assurance records as required.
Adhere to all quality and safety standards, as well as ensuring compliance with all applicable regulatory agencies.
Work closely and communicate with other lab associates to complete daily activities efficiently.
Maintain other Clinical Laboratory databases as needed or assigned.
Provide administrative support for Clinical Laboratory projects as needed.
Represent department and the organization favorably and in accordance with established Company standards and associate attributes at all times.
Ensure adherence to laboratory safety policies
Manage issues and projects; resolve escalated issues as appropriate.
Demonstrate superior understanding of Laboratory operations and department processes.
Suggest potential improvements to existing systems and processes to immediate supervisor.
Help to develop and provide training to new and existing associates on department functions.
Organize and analyze data entry errors to help determine opportunities for individual performance and process improvement.
Participate in identifying solutions regarding data entry errors and concerns.
Help with weekly scheduling of staff.
Serve as the primary trainer for new LDEQCR or re-training of existing LDEQCR
Accurately answer questions when Supervisor is unavailable.
Interact with other departments as necessary and develop relationships with other Lab Leadership and Management as it relates to work processes and workflow.
Communicate concerns/needs as necessary to Supervisor.
Aid Supervisor with areas of improvement in workflow or organization