Job Description

Function Specific
\xef\x82\xb7 Demonstrate the ability to multi-task and manage Specimen Test Plan(STP)s across multiple client instances.
\xef\x82\xb7 Plan and establish timelines to meet or exceed business expectations for STPs/review schedules.
\xef\x82\xb7 Allocate time for investigation and resolution implementation.
\xef\x82\xb7 Strong troubleshooting and analytical skills for identification of errors and resolution steps.
\xef\x82\xb7 Utilize strong working knowledge of SOPs, validation standards, and work procedures to suggest potential improvements and to provide training and guidance to all staff.
\xef\x82\xb7 Support management of metrics.
\xef\x82\xb7 Assist with investigating or resolving issues of quality as directed.
\xef\x82\xb7 Suggest process improvements where issues are seen.
Customer Facing
\xef\x82\xb7 There are basic customer interface job functions in this position.
Metrics
\xef\x82\xb7 Support management for metrics.
\xef\x82\xb7 Assist with investigating or resolving issues of quality as directed.
Staff and Financial Management
\xef\x82\xb7 Understand implications of activities to project budgets.
Process Improvement
\xef\x82\xb7 Suggest process improvements where issues are seen.
\xef\x82\xb7 Support Six Sigma process improvement teams.
Training / SOPs
\xef\x82\xb7 Reviews training materials for staff.
\xef\x82\xb7 Mentor and support other GSS employees in their understanding and adoption of STP to GlobalCODE\xc2\xae.
\xef\x82\xb7 Active member of SOP review teams as assigned.
Other
\xef\x82\xb7 Lead or assist with special projects as designated.
\xef\x82\xb7 Perform other duties as assigned by management.Experience:Minimum Required:
\xef\x82\xb7 Minimum 2-3 years of experience working in clinical trials, laboratory, or specimen management, central lab setup is preferred. Informed consent and regulatory knowledge, molecular biology, clinical pharmacogenomics or biomarker research experience are all a plus
\xef\x82\xb7 Proven ability to plan, prioritize, and manage in a fast-paced environment with a high degree of initiative
\xef\x82\xb7 Strong drive for process optimization and data integrity
\xef\x82\xb7 Excellent communication and interpersonal skills
\xef\x82\xb7 Detail oriented, ability to work independently and ability to work/communicate effectively with clients
\xef\x82\xb7 Experience with 21 CFR Part 11 in a pharmaceutical, biotechnology, CRO or related industry
\xef\x82\xb7 Ability to work in a rapidly changing environment
\xef\x82\xb7 Independently analyze, solve, and correct issues in real time, providing problem resolution end-to-end.
\xef\x82\xb7 Strong MS/Office skills in particular with Excel and Word.
\xef\x82\xb7 In addition to above, candidates with relevant domain knowledge or experience may be considered, if deemed appropriate for specific tasks and activitiesEducation/Qualifications/Certifications and LicensesMinimum required:
\xef\x82\xb7 University/College Degree (Life Science preferred), or certification in an allied health profession from an appropriate accredited institution (Ex: Nursing certification, Medical or laboratory technology) and 1-2 years of work experience in clinical research industry, laboratory, or specimen management
\xef\x82\xb7 In addition to above, Candidates without life sciences background but with relevant domain knowledge or experience may be considered, if deemed appropriate for specific tasks and activities.Labcorp is proud to be an Equal Opportunity Employer:As an EOE/AA employer, Labcorp strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply.For more information about how we collect and store your personal data, please see our .

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