Clinical Laboratory Associate
Durham, North Carolina, United States
Expertise in end-to-end delivery of analytical and pre-analytical lab services to support clinical trials in a CRO environment. Includes kit receipt, specimen management, specimen preparation and lab analysis across a broad spectrum of methods and technologies.Responsible for performing a variety of routine testing procedures to obtain data for use in clinical trials research. Skills: Maintain records of processing, compliance with Good Manufacturing Practice (GMP)/Good Clinical Practice (GCP), Standard Operating Procedures (SOP's), Good Laboratory Practice (GLP) and CAP/CLIA regulations.Facilitating process enhancements throughout various Gene Expression assays, teams, and company-wide initiatives, concurrently fostering a positive and collaborative culture among team members.Experience includes: Troubleshooting Clinical Trials, 10X Genomics System/Single Cell Sequencing. Library Preparation (GEX, TCR, BCR), Next Generation Sequencing (Illumina, Ion Torrent) & analysis, RNA/DNA Isolation, qPCR, NanoString Sample Preparation for Gene Expression Analysis, Sanger Sequencing, Biomarker Determination, Targeted DM1 Sequencing Panel.