What are the responsibilities and job description for the Laboratory Data Entry Quality Control Review - Tuesday-Saturday 8:00am-4:30pm position at Eurofins Clinical Diagnostics?
Job Description
Eurofins Viracor LLC is an equal opportunity employer and encourages individuals from all backgrounds to apply. By submitting your application, you acknowledge and agree to the following conditions:
Drug Screen: Successful candidates will be required to pass a standard drug screen as part of the pre-employment process.
Background Check: A thorough background check will be conducted for all potential employees. This may include, but is not limited to, criminal history, education verification, and employment history.
Visa Sponsorship: Eurofins Viracor LLC does not sponsor employment visas. All candidates must have the legal right to work in Lenexa, KS without requiring sponsorship. Unless approved by HR and supporting parties.
Basic Function And Scope Of Responsibility
The Laboratory Data Entry QC Review associate is responsible for the review and audit of order entry information and performing duties with a high degree of proficiency. The Laboratory Data Entry QC Review associate is also responsible for performing duties related to accessioning and data entry.
Essential Job Duties
Level I - Minimum
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.
Other duties as assigned by management.
Level II – Fully meets the qualifications of Level I plus the following:
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.
Level III – Fully meets the qualifications of Level II plus the following:
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.
Eurofins Viracor LLC is an equal opportunity employer and encourages individuals from all backgrounds to apply. By submitting your application, you acknowledge and agree to the following conditions:
Drug Screen: Successful candidates will be required to pass a standard drug screen as part of the pre-employment process.
Background Check: A thorough background check will be conducted for all potential employees. This may include, but is not limited to, criminal history, education verification, and employment history.
Visa Sponsorship: Eurofins Viracor LLC does not sponsor employment visas. All candidates must have the legal right to work in Lenexa, KS without requiring sponsorship. Unless approved by HR and supporting parties.
Basic Function And Scope Of Responsibility
The Laboratory Data Entry QC Review associate is responsible for the review and audit of order entry information and performing duties with a high degree of proficiency. The Laboratory Data Entry QC Review associate is also responsible for performing duties related to accessioning and data entry.
Essential Job Duties
Level I - Minimum
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.
Other duties as assigned by management.
Level II – Fully meets the qualifications of Level I plus the following:
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.
Level III – Fully meets the qualifications of Level II plus the following:
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.
