Qiuxia Chen

Qiuxia Chen

Senior Director

About

• Extensive experience in early discovery of small molecule drugs in different therapeutic areas; familiar with discovery biology and innovative screening platforms, particularly DNA-endcoded library. • Strong expertise in assay development, biochemistry, cellular and molecular biology, signaling transduction, identification and validation of both protein and non-canonical targets. • Working knowledge of method development (HPLC, FPLC and LC/MS), protein sciences, PROTAC, drug metabolism, and ADME. • Excellent troubleshooting, multitasking and interpersonal skills, capable of critical thinking, working independently or as a team member/leader. Experimental skills: • Biochemical Assays: enzyme kinetics, small molecule screening, MOA study, FP, FRET, Alpha tech, Luminescence, ELISA. • Biophysical Assays: TSA, SPR, ITC, BLI, TRIC • DNA encoded library screening • Cell Biology: Cell culture, Cell poliferation assay, Cell signaling assay, FACS analysis • Molecular Biology: Prepping DNA/RNA samples from cell culture or tissue. DNA subcloning, transfection, cell line establishment, PCR, qRT -PCR, Western blot, EMSA, ELISA, confocal microscopy, tissue section, luciferase reporter gene assay, DNA/RNA NGS sequencing. • Analytical Chemistry: HPLC/MS, FPLC • Animal experiment: hands-on experience with rodent models of efficacy and ADME evaluation

Country

China

City

Chengdu

Industry

Hospital & Health Care

Skill

Cell Biology, Molecular Biology, Cell Culture, Molecular Cloning, LC-MS, HPLC, Drug Discovery, RNA Biology, Animal Handling, RNAi, FPLC, DNA encoded library, Biophysical assay, Biochemical assay, Cellular Assays

Experience

Chengdu New Radiomedicine Technology

Senior Director

Chengdu New Radiomedicine Technology

2024-8 - Present · 2 yrs 2 mos

Chengdu, Sichuan, China

Biochemical, biophysical and cellular assay • Establish and optimize assays for targets in radioligand therapy. • Lead in vitro biology team. Project management for radiopharmaceutical development • Conduct background research on potential drug targets. • Lead project, define scope and go/no-go decision points. • Organize internal resources and coordinate with CROs, ensure that all projects are on-schedule.

HitGen Inc.

Senior Biologist to Director

HitGen Inc.

LinkedIn
2016-2 - 2024-8 · 8 yrs 7 mos

Chengdu, Sichuan, China

Biochemical, biophysical and cellular assay • Establish and optimize assay protocols for novel targets. • Small molecule evaluation and MOA study. DNA encoded library (DEL) screening • DEL selection of different targets • DEL selection optimization and innovation Project management • Manage DEL screening projects, design experiment plan. • Organize and coordinate internal resources, ensure that all projects are delivered on-time. • Manage the relationship with the client.

University of California, Davis

Junior Specialist

University of California, Davis

LinkedIn
2013-7 - 2015-3 · 1 yr 9 mos

Sacramento, California Area

Department of Biochemistry and Molecular Medicine 07/2013-03/2015: High-yield biosynthesis of chimeric RNAs bearing various types of functional small RNAs for broad applications • developed a novel strategy to achieve consistent high-yield biosynthesis of chimeric RNAs carrying various small RNAs (miRNAs, siRNAs and RNA aptamers) • performed deep RNA sequencing analyses and revealed that mature miR-124 and target GFP-siRNA were selectively released from chimeric RNAs in human cells. • miR-124, GFP-siRNA and malachite green aptamer released from chimeric RNAs were proved functional in either cell or animal study. • developed a specific and label-free method to determine serum RNase activities in pancreatic cancer patients. 07/2013-09/2014: Recombinant human pre-miRNA-34a as novel cancer therapeutics • biosynthesis of human pre-miRNA-34a agents in Escherichia coli. • rapid purification of recombinant RNA using FPLC. • suppression of cell proliferation and xenograft tumors growth in animal models by pre-miRNA-34a. 07/2013-04/2014: hsa-miR-1291 function Study • tested the expression of hsa-miR-1291in different cell lines by qRT-PCR. • constructed UTR reporter plasmids, performed luciferase assay and western blot to determine the target of hsa-miR-1291.

University at Buffalo

Visiting PHD Student

University at Buffalo

LinkedIn
2012-10 - 2013-4 · 7 mos

Buffalo/Niagara, New York Area

Evaluation of cationic polylactide(CPLA) as carriers for gene delivery • tested transfection efficiency of CPLA54 by using different weight ratios of the PhrGFP II-1/CPLA54 complex. • determined toxicity of CPLA54 in different cell lines. • investigated the capacity of CPLA54 as a nanocarrier for micrRNA expression in comparison to lipofectamine2000.

Education

Zhejiang University

Zhejiang University

LinkedIn

Pharmaceutical Sciences

2010 - 2015 · 5 yrs

Pharmaceutical Analysis, College of Pharmaceutical Sciences 09/2011-10/2012:Mechanism involded in P-gp(MDR1) induction by vinblastine • established vinblastine resistant Caco-2 cells. • assayed AP-1 and NF-kB luciferase activity in vinblastine resistant and wild type Caco-2 cells. • tested the inhibition of MDR-1mRNA expression by c-jun and NF-kB inhibitors. 07/2010-07/2011:Establishment of LLC-PK1 Cell Line Expressing P-gp 03/2010-06/2010:Establishment of MDCK-MDR1 Cell Line Expressing CYP3A4

Sichuan University

Sichuan University

LinkedIn

Pharmaceutical Sciences

2006 - 2010 · 4 yrs

West China School of Pharmacy

Qiuxia Chen's Contact Information

Email

******@***.com

Phone

(**) *** ****

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