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Medical University of South Carolina (MUSC - Univ) seeks a Laboratory Technologist II to perform complex molecular tests and manage samples for SCTR Research Nexus approved clinical trials. You will ensure proper procurement, processing, banking, and shipping of study samples with rigorous data entry and record-keeping.
The role requires adherence to laboratory safety practices and compliance with MUSC, SCTR, state and federal guidelines while supporting investigators and study teams.
Under direct/general supervision of the Research Laboratory Manager, the Laboratory Technologist II performs complex laboratory tests and molecular laboratory procedures to support SCTR Research Nexus approved clinical trials. Responsible for performing study participant sample procurement, processing, banking, and shipping according to clinical trial documents. Performs complex procedures as required by approved protocols. Performs accurate and timely data entry and record keeping in sample database, and maintain all records relating to clinical trial lab management. Responds appropriately to clinical trial study team inquires in a timely manner. Knowledge of laboratory facilities, methods, equipment, materials, and laboratory safety practices, as well as human subjects research. Responsible for compliance with study requirements as well as all MUSC, SCTR, state and federal guidelines.
Entity
Medical University of South Carolina (MUSC - Univ)
Worker Type
Employee
Worker Sub-Type
Research Grant
Cost Center
CC001064 COM SCTR Operations CC
Pay Rate Type
Hourly
Pay Grade
University-GEN09
Pay Range
53,142.00 - 71,706.00 - 90,372.000
Scheduled Weekly Hours
40
Work Shift
Job Description:
Under direct/general supervision of the Research Laboratory Manager, the Laboratory Technologist II performs complex laboratory tests and molecular laboratory procedures to support SCTR Research Nexus approved clinical trials. Responsible for performing study participant sample procurement, processing, banking, and shipping according to clinical trial documents. Performs complex procedures as required by approved protocols. Performs accurate and timely data entry and record keeping in sample database and maintain all records relating to clinical trial lab management. Responds appropriately to clinical trial study team inquires in a timely manner. Knowledge of laboratory facilities, methods, equipment, materials, and laboratory safety practices, as well as human subjects research. Responsible for compliance with study requirements as well as all MUSC, SCTR, state and federal guidelines.
Minimum Requirements: A bachelor's degree in a related medical or scientific discipline; or an associate degree or equivalent technical training in a related medical, scientific or technical discipline and two years journey-level work experience in a related field.
Physical Requirements: (Note: The following descriptions are applicable to this section: Continuous - 6-8 hours per shift; Frequent - 2-6 hours per shift; Infrequent - 0-2 hours per shift) Ability to perform job functions in an upright position. (Continuous) Ability to p