Processing Tech I, II Clinical Trials and Pharma

Arup; Salt Lake City (UT); On-site; USD 49,594,000 - 55,104,000; Full time

Job summary

ARUP Laboratories, a national clinical and anatomical pathology reference laboratory based in Salt Lake City, UT, seeks a Processing Tech I, II for Clinical Trials and Pharma. The role handles receipt, shipment manifesting, and processing of research specimens, with emphasis on accuracy, compliance, and coordination with internal teams.

Schedule: 7-On/7-Off B week, 8:00 AM - 6:30 PM. Open to individuals who value safety, documentation, and efficient specimen handling in a fast-paced environment.

Qualifications

• Must be able to type 30 WPM.
• Must successfully pass the departmental competency testing exam with a score of 90% or higher.
• Must maintain department quality requirements.

Responsibilities

• Open, evaluate, and process inbound shipments using ARUP shipment tracking applications.
• Ensure specimens are prioritized and processed promptly.
• Add and verify temperature-controlled materials as appropriate.
• Evaluate shipments for late priority, temperature compliance, and special handling.
• Monitor and manage Special Needs Requests and Short Stability Reports.
• Distribute shipments to Innovation teams as required.
• Process specimens across temperature conditions and route appropriately.
• Coordinate with processing, automated systems, or laboratories to ensure timely delivery.
• Enter patient demographics and accession specimens using ARUP applications.
• Order tests as indicated on requisitions and process orders.
• Label and de-identify specimens and requisitions.
• Verify specimen identifiers and paperwork for accuracy and discrepancies.

Skills

Typing 30 WPM

Attention to detail

Team collaboration

Education

High School Diploma or Equivalent

Job description

Processing Tech I, II Clinical Trials and Pharma

Job Category : Clinical Support

Requisition Number : PROCE023218

• Full-Time
• On-site
• Rate : $17.53 USD per hour

Locations

Showing 1 location

Salt Lake City, UT 841081221, USA

Description

Schedule:
7-On/7-Off B week
8:00 AM - 6:30 PM

Primary Purpose

Works under general supervision to ensureaccuratereceipt, handling, shipment manifesting, and processing of all research specimens received at ARUP's central facility.This position supports Clinical Trials Sample Management (CTSM) operations through shipment manifesting, specimen accessioning, data entry, aliquoting, special handling and coordination with internal laboratories and Innovation project management groups. The role requires the ability to process specimens across temperature types, ensure proper documentations and compliance with departmental procedures, and to support resolution of routine shipping and specimen issues.

About ARUP

ARUP Laboratories is a national clinical and anatomic pathology reference laboratory and an enterprise of the University of Utah and its Department of Pathology. Based in Salt Lake City, Utah.

ARUP proudly hires top talent to create a work environment of diversity, professional growth and continuous development. Our workforce is committed to the important service we provide to over one million patients each month. We always strive for excellence and have a strong desire to have involvement with the advances in medicine and the role laboratory services plays within each patient’s life. We never forget that there is a patient behind every specimen we receive.

We are looking for individuals who want to contribute to ARUP's culture of accountability, integrity, service, and excellence. Consider joining our dynamic team.

Essential Functions

Open, evaluate, and process inbound shipments using ARUP shipment tracking applications.

Ensures specimens are prioritized appropriately and processed promptly.

Adds and verifiestemperature ‑ controlmaterials (e.g., dry ice) asappropriate.

Evaluates shipments for late priority, temperature compliance, and special handling requirements.

Monitors and manages Special Needs Requests, Short Stability Reports, and flagged specimens.

Distributes Local, Room Temperature, FedEx, and isolated shipments to Innovation teams asrequired.

Processes specimens across all three temperature conditions and routes to automated or manual systems accordingly.

Coordinates with Specimen Processing, automated systems, or testing laboratories to ensuretimelydelivery.

Specimen Receipt & Processing

Promptly process specimens as they become available following established corporate and departmental procedures.

Evaluates inbound shipments;documentsshipping discrepancies, temperature excursions, and other specimen acceptability violations.

Ensures all specimens andaccompanyingdocumentationmeetidentification, labeling, and matching requirements.

Enter patient demographics andaccessionspecimens usingappropriate ARUPapplications, ensuring accuracy and completeness.

Orders tests asindicatedon requisitions and processes both manual and electronically transmitted orders.

Properly labelsdeidentifiedspecimens and requisitions.

Verify all specimen identifiers, labels, and paperworkmatchboth physically and electronically, documenting discrepancies per procedure.

Recognizes and appropriately handles all specimen types and prioritizations.

Aliquots specimens using the proper safety equipment and procedures.

Properly documents all specimenreceiptand client provided information per policy.

Processes specimens requiring rerouting or shared handling appropriately.

Operates centrifuges and biological safety cabinets asrequired.

Systems, Tools, & Documentation

Proficient in ARUP applications including accessioning, inquiry, shipment tracking, checkout, and applicable LIS platforms.

Utilizes the Internal Test Directory (ITD) to supportaccessioningand team inquiries.

Uses ARUPauto ‑ orderingapplications to ensureaccurateand complete order uploads.

Maintainsaccuratedocumentation and comments foraccessioningandshipmentrecords.

Quality, Safety, & Compliance

Adheres to ARUP safety policies, specimen handling requirements, and PPE standardsin accordance withCDC and OSHA regulations.

Observes data security and patient confidentiality principles.

Maintains ethical standards in interactions with coworkers and visiting clients.

Supports Quality Review activities as assigned.

Maintains department quality, productivity, and reliability expectations.

Facilitates communication between team members, project managers, and internal laboratories as needed.

Exercises sound judgment andescalatesissues to senior staff whenappropriate.

General Duties

Ensures workstations are clean, stocked, and compliant with safety standards.

Performs routine cleaning duties andassistswith departmental projects.

Remains informed of current departmental specimen processing and manifesting procedures.

Other duties as assigned.

Physical and Other Requirements

Stooping: Bending body downward and forward by bending spine at the waist.

Reaching: Extending hand(s) and arm(s) in any direction.

Mobility: The person in this position needs to move between work sites and inside the office to access file cabinets, office machinery, etc.

PPE: Biohazard laboratory environment that requires use of personal protective equipment in accordance with CDC and OSHA regulations and company/departmental policies.

ARUP Policies and Procedures: To conduct self in compliance with all ARUP Policies and Procedures.

Abide by the Code of Conduct as outlined in the ARUP employee handbook.

Medium Work: Exerting up to 50 pounds of force occasionally, and/or up to 30 pounds of force frequently, and/or up to 10 pounds of force constantly to move objects.

Fine Motor Control: Picking, pinching, typing or otherwise working, primarily with fingers rather than with the whole hand as in handling.

Vision: Having close, far, and peripheral visual acuity to perform a variety of tasks such as make general observations of depth and distance.

Color Vision: Perception of and ability to distinguish colors

Regular and reliable attendance.

Reliable and dependable performance.

Ability to work well with others.

Ability to work all required overtime.

Qualifications

Education

Required

High School Diploma or Equivalent or better.

Experience

Required

Must be able to type 30 WPM

After completion of training, must successfully pass the departmental competency testing exam with a score of 90% or higher

Must be able to maintain department quality requirements

Preferred

Processing at or above 20 specimens or tests per hour (using the department’s productivity report), and not exceed the departmental threshold for errors or attendance infraction issues OR 3 years at ARUP in a Technical Operations role

Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities
This employer is required to notify all applicants of their rights pursuant to federal employment laws.For further information, please review the Know Your Rights notice from the Department of Labor.