Position Title: Clinical Laboratory Scientist
Location: Old Hwy 75 Butner, NC 27509
Duration: 12 Months
Work Schedule: An anticipated schedule for the provision of contract services is 8 hours per day, Sunday through Saturday, including federal holidays. This anticipated schedule includes a 30 minute unpaid lunch break when working 8 hours per day.

TO BE CONSIDERED FOR THIS POSITION, YOU SHOULD HAVE: [SKILLS, EDUCATION, OR EXPERIENCE]

• All contractors provide documentary evidence of completion of a clinical laboratory training program.
• All contractors must provide documentary evidence of completion of clinical laboratory certification exam.
• All contractors must provide documentary evidence of experience within the past three (3) years in preforming clinical laboratory testing on human specimens.
• All contractors must have the ability to work with inmates. The contractors will work with an inmate population from a variety of cultural, regional, racial, religious, and ethnic backgrounds. Experience

working with an inmate population preferred, but not required.

• All contractors will provide documentary evidence of CPR certification.

Tryfacta is an Equal Opportunity/Affirmative Action Employer.
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, protected veteran or disabled status, or genetic information.

• The contractor shall provide professional clinical laboratory testing services to inmates.
• The contractor will function as a generalist performing testing in all disciplines of the clinical laboratory including hematology, transfusion services, coagulation, urinalysis, infectious disease, serology, and chemistry.
• The nature of the work demands an advanced thorough knowledge of clinical laboratory sciences as they relate to the performance of laboratory analysis on human blood, tissues, and body fluids.
• A specialized knowledge of clinical correlation which relates laboratory test data to human physiology, a broad knowledge of laboratory testing methodologies, laboratory equipment/instrumentation maintenance and quality assurance procedures is required.
• Experience in performing external proficiency testing programs to maintain accreditation of the laboratory. Experience in conducting quality control procedures on equipment, reagents, and products by implementing instrument, reagent, and product testing systems. The contractor shall be responsible for, but not limited to the following tasks: ordering laboratory studies in the Laboratory Information System, drawing blood samples on ordered studies, preparing samples for processing, sharps accountability, maintaining logs and records, filling out appropriate laboratory request forms, preparation of the call out (draw list and labels), maintenance of a waiting list, restocking supplies as needed, daily maintenance of laboratory equipment, including advising the Laboratory Supervisor when equipment requires professional maintenance or repair, biological specimen preparation and packaging for shipment to contract laboratories, processing incoming referral specimens, processing outgoing specimen containers to referral facilities, maintenance of laboratory logs and other records as necessary for complying with Clinical Laboratory Improvement Amendment (CLIA) guidelines, informing the Laboratory Supervisor of all information pertaining to the services rendered, i.e., specimen(s) obtained, and reporting any problems arising in regards to laboratory services. Normally, the duties of the contractor would not require direct entries in the inmate’s medical record. However, some information generated by the contactor may be included in the inmate’s medical record. The contractor is responsible for providing technical and clerical support to the laboratory.