Summary
Overview
Work History
Education
Skills
Languages
ADDITIONAL STRENGTHS
Timeline
Generic

Nazanin Mokhtarpour

Redmond,WA

Summary

Analytical scientist with experience in method development, LC-MS/MS, HPLC, and regulated bioanalytical workflows supporting drug development. Background includes method qualification, troubleshooting, stability testing, and supporting technology transfer activities. Strong documentation skills with experience in GMP-aligned environments, QC laboratory operations, and cross-functional collaboration with R&D, QA, and external partners. Interested in nanoparticle formulation, analytical control strategies, and bridging R&D methods into GMP readiness.

Overview

8
8
years of professional experience

Work History

Bioanalytical Scientist II

Medpace Bioanalytical Laboratories
Cincinnati, OH
12.2024 - 06.2026
  • Developed, optimized, and executed analytical methods (LC-MS/MS, HPLC) to support clinical and nonclinical studies, including identity, purity, and stability assessments.
  • Performed sample preparation (protein precipitation, LLE, SPE) and executed routine and non-routine analytical testing with strong troubleshooting capability.
  • Supported method qualification and transfer activities, contributing to transfer documentation, data packages, and communication with partner labs.
  • Conducted PK sample analysis, calibration curve generation, QC evaluation, and data verification to ensure data integrity.
  • Maintained GMP-aligned documentation, including protocols, validation reports, controlled records, and experimental summaries.
  • Collaborated with QA, project managers, and scientific teams to support program timelines and analytical readiness.
  • Performed instrument maintenance, calibration, and performance monitoring to ensure analytical reliability.

Bioanalytical Scientist I

Medpace Bioanalytical Laboratories
Cincinnati, OH
10.2022 - 12.2024
  • Developed and validated analytical methods for small-molecule drug candidates, supporting formulation and process development activities.
  • Executed stability studies, impurity profiling, and characterization experiments to support formulation screening and process optimization.
  • Assisted with tech transfer preparation, including drafting method transfer protocols and supporting comparability assessments.
  • Maintained high-quality experimental records and contributed to technical reports and cross-functional data reviews.
  • Supported QC-related activities including batch documentation review, data verification, and deviation investigation support.

Research Assistant

University of Cincinnati
Cincinnati, OH
08.2019 - 12.2022
  • Conducted organic synthesis of small molecules, including multi-step reaction design, purification, and structural characterization.
  • Characterized compounds using MALDI-TOF, NMR, UV-Vis, ITC, and chromatographic techniques.
  • Performed protein–ligand interaction studies and supported structure–activity relationship (SAR) analysis.
  • Designed and optimized synthetic routes and analytical workflows to support medicinal chemistry programs.
  • Prepared technical reports, manuscripts, and scientific presentations.
  • Maintained detailed laboratory records and contributed to method optimization.

Graduate Research Assistant

Mississippi State University
Starkville, MS
01.2018 - 12.2018
  • Designed and executed organic synthesis experiments, including reaction setup, monitoring, purification, and characterization.
  • Characterized compounds using GC-MS, IR spectroscopy, and other analytical tools.
  • Developed laboratory SOPs and supported experimental design, data analysis, and documentation.

Education

Ph.D. - Medicinal Chemistry

University of Cincinnati
Cincinnati, OH
01-2022

M.Sc. - Organic Chemistry

Ferdowsi University of Mashhad
Mashhad, Iran
01-2015

B.Sc. - Chemistry

University of Mazandaran
Iran
01-2013

Skills

  • Analytical Method Development & Qualification
  • LC-MS/MS, HPLC, GC-MS, ICP-MS
  • Stability Studies & Characterization
  • Method Transfer & Tech Transfer Support
  • GMP/GDP Documentation Practices
  • QC Laboratory Operations
  • Cross-Functional Collaboration (R&D, QA/QC, CDMOs)
  • Troubleshooting & Data Interpretation
  • Sample Preparation (PPT, LLE, SPE)
  • Experimental Design & Process Support
  • Organic Chemistry: Multi-step synthesis, reaction optimization, purification, structural elucidation
  • Analytical Techniques: HPLC/UPLC, LC-MS/MS, GC-MS, NMR, MALDI-TOF, ITC, UV-Vis, FTIR
  • Software: Analyst, Sciex OS, Empower, MS Office, statistical tools
  • Documentation: SOPs, validation reports, regulatory documentation
  • Regulatory: GLP/GMP, method lifecycle documentation, data integrity (ALCOA)

Languages

English
Native or Bilingual

ADDITIONAL STRENGTHS

  • Strong scientific judgment and troubleshooting ability
  • Excellent communication skills for leading cross-functional discussions
  • Ability to manage multiple priorities in fast-paced environments
  • High attention to detail and commitment to quality

Timeline

Bioanalytical Scientist II

Medpace Bioanalytical Laboratories
12.2024 - 06.2026

Bioanalytical Scientist I

Medpace Bioanalytical Laboratories
10.2022 - 12.2024

Research Assistant

University of Cincinnati
08.2019 - 12.2022

Graduate Research Assistant

Mississippi State University
01.2018 - 12.2018

M.Sc. - Organic Chemistry

Ferdowsi University of Mashhad

B.Sc. - Chemistry

University of Mazandaran

Ph.D. - Medicinal Chemistry

University of Cincinnati
Nazanin Mokhtarpour