LabCorp is searching for a Project Specialist to join their team in RTP, NC! You will play a vital role in ensuring the successful execution of projects for the Cytogenetics group. Working closely with a dynamic team, you will contribute to the planning, coordination, and execution of change management aimed at advancing Cytogenetics diagnostics and healthcare solutions.
Work Schedule: 1st shift, Monday-Friday, 8:00am-4:30pm.
Benefits: Employees regularly scheduled to work 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(k), Paid Time Off (PTO) or Flexible Time Off (FTO), Tuition Reimbursement and Employee Stock Purchase Plan. Casual, PRN & Part Time employees regularly scheduled to work less than 20 hours are eligible to participate in the 401(k) Plan only. For more detailed information, please click here.
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Job Duties/Responsibilities:
- Performs assigned activities of project team, and works with the supervisors, managers and directors on planning, initiating and completing all assigned Change Controls.
- Analyzes existing forms and methods to promote effective operations through standardization, simplification, discontinuance or other methods; installs new systems or procedures in various departments and instructs personnel regarding them.
- Serves as a subject-matter expert for assigned assays
- Generates complete, accurate and timely correspondence such that the reader understands the intended message.
- Performs administrative support duties (e.g. maintains records, generates and/or sends reports and communications, maintains databases, enters data, answers phones, files, etc.) completely, accurately and within established timeframes.
- Assists supervisor/manager in performing various assigned responsibilities (i.e. planning, compliance, troubleshooting, training, making workflow recommendations, etc.) completely, accurately and within established timeframes.
- Performs designated QA testing for developed (products, reports, interfaces, modules, training materials, etc.) before they are released for use.
- Coordinates work/information between designated parties and ensures optimal performance such that objectives and goals are achieved completely and accurately.
Requirements:
- Bachelor's degree in a Chemical or Biological science, Clinical Laboratory Science, Medical Technology or meet local regulatory (CLIA & State) requirements.
- A minimum of 1 year of clinical laboratory testing experience with human specimens is required OR an MLS degree.
- AMT or ASCP certification preferred.
If you're looking for a career that offers opportunities for growth, continual development, professional challenge and the chance to make a real difference, apply today!
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
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