Clinical Laboratory Technologist IV / V / VI #4837 #4838 #4839 #4840 #4841 #4842 ((Night Shift,

Responsibilities

• Perform testing activities according to established laboratory procedures, study protocols, and quality standards to support clinical research and safety study objectives.
• Prepare samples, reagents, materials, and work areas in accordance with defined workflows, ensuring accurate labeling, traceability, and compliant handling throughout the testing process.
• Operate and maintain laboratory instruments by performing routine checks, calibrations, and basic troubleshooting steps, and report equipment concerns to appropriate personnel.
• Record and verify test data in laboratory systems with accuracy and completeness, following defined documentation practices and data integrity expectations.
• Review assay results for consistency within expected ranges, identify routine inconsistencies, and escalate unusual findings to senior team members for further evaluation.
• Follow established procedures for quality control activities, including running controls, documenting deviations, and supporting routine review of quality trends.
• Support the coordination of study activities by ensuring appropriate sample flow, materials availability, and completion of required documentation according to defined requirements.
• Participate in verification activities for new equipment, procedures, or reagent lots by performing assigned tasks in accordance with established protocols.
• Maintain a clean and organized work environment by following laboratory safety, biosafety, and housekeeping practices required for regulatory readiness.
• Collaborate with team members by sharing information related to task progress, workflow timing, and procedural requirements to support consistent laboratory operations.

Required Qualifications

• Bachelor’s degree in a life science field with relevant laboratory experience.
• ASCP MLS/MT or equivalent preferred.
• Demonstrated level of knowledge regarding applicable regulatory standards commensurate with the position's complexity and scope, contributing to organizational regulatory compliance.

Preferred Qualifications

• Proficiency in molecular testing workflows and basic troubleshooting.
• Strong time management skills to balance multiple test runs.
• Ability to coach less experienced team members.
• Working knowledge of CLIA/CAP documentation requirements.