Research Associate - DMPK / Bioanalysis

MEDICILON USA CORP
  • Lexington, MA
  • Full-time
3 days ago

Job Description

Benefits:
  • 401(k) matching
  • Dental insurance
  • Health insurance
  • Paid time off
  • Training & development
  • Vision insurance

Medicilon USA Corp is seeking a motivated and detail-oriented Research Associate to join our DMPK and Bioanalysis team in Lexington, MA. This is a hands-on laboratory role supporting preclinical drug discovery and development, with a primary focus on bioanalytical sample preparation, LC-MS/MS, and quantitative analysis.


The ideal candidate will have practical experience in analytical chemistry, bioanalysis, or DMPK, with a strong understanding of laboratory techniques and biological sample processing. This individual will work closely with Scientists and cross-functional teams to support pharmacokinetic (PK), toxicokinetic (TK), pharmacodynamic (PD), biomarker, and biodistribution studies across multiple therapeutic modalities.


Key Responsibilities


  • Perform bioanalytical sample preparation and quantitative analysis of biological matrices, including plasma, serum, urine, and tissue samples.
  • Support LC-MS/MS method development, optimization, and analysis of small molecules, biologics, oligonucleotides, and other therapeutic modalities.
  • Perform sample preparation techniques, including protein precipitation, liquid-liquid extraction, and solid-phase extraction (SPE).
  • Prepare calibration standards, quality control samples, reagents, and study samples.
  • Operate, maintain, and troubleshoot LC-MS/MS, HPLC, and other analytical laboratory instruments.
  • Process, analyze, and summarize experimental data using Analyst, Excel, GraphPad Prism, or other relevant software.
  • Support bioanalytical studies for PK, TK, PD, biomarkers, and biodistribution.
  • Assist with additional bioanalytical platforms, including ELISA/MSD, ligand-binding assays, qPCR/ddPCR, and cell-based assays, as needed.
  • Support in vitro ADME assays, including metabolic stability, plasma protein binding, permeability, and drug-drug interaction (DDI) studies.
  • Maintain accurate laboratory records and documentation in accordance with established SOPs, study protocols, and applicable GLP/GxP requirements.
  • Assist with data interpretation, study reports, and technical documentation.
  • Collaborate with Scientists and project teams to ensure accurate, efficient, and timely study execution.
Qualifications


  • Bachelor's or Master's degree in Analytical Chemistry, Chemistry, Biochemistry, Pharmaceutical Sciences, Pharmacology, Biology, or a related field.
  • 1–3 years of relevant laboratory experience in bioanalysis, analytical chemistry, DMPK, pharmaceutical research, or a related field.
  • Hands-on experience with LC-MS/MS and/or HPLC instrumentation.
  • Experience with biological sample preparation and processing, including plasma, serum, urine, or tissue samples.
  • Understanding of chromatographic techniques, mass spectrometry, and quantitative bioanalytical methods.
  • Familiarity with laboratory data analysis, documentation, and quality control procedures.
  • Strong attention to detail, organizational skills, and ability to follow established experimental protocols and SOPs.
  • Good communication, problem-solving, and teamwork skills.
  • Ability to work independently on assigned laboratory tasks while collaborating effectively with a multidisciplinary team.
Preferred Qualifications


  • Previous experience in a CRO, pharmaceutical, or biotechnology laboratory environment.
  • Experience with LC-MS/MS method development, optimization, qualification, or validation.
  • Experience with bioanalysis of small molecules, oligonucleotides, biologics, or other novel therapeutic modalities.
  • Familiarity with ELISA/MSD, ligand-binding assays, qPCR/ddPCR, or cell-based assays.
  • Knowledge of GLP principles and FDA/EMA bioanalytical method validation guidelines.
  • Experience with in vitro ADME assays or PK data analysis using Phoenix WinNonlin.
  • Hands-on experience supporting in vivo rodent studies, including animal handling, compound dosing, blood collection, necropsy, and tissue harvesting.
  • Experience processing biological samples collected from in vivo studies for downstream bioanalytical analysis.
 

Numbers & Facts

LocationLexington, MA
Job TypeFull-time

Skills

  • Analysis Skillsunmatched
  • Analytical Chemistryunmatched
  • Assaysunmatched
  • Biochemistryunmatched
  • Biologyunmatched
  • Biomarkersunmatched
  • Biotech and Pharmaceuticalunmatched
  • Blood Bankunmatched
  • Calibrationunmatched
  • Chromatographyunmatched
  • Clinical Researchunmatched
  • Communication Skillsunmatched
  • Contract Research Organization (CRO)unmatched
  • Cross-Functionalunmatched
  • Data Analysisunmatched
  • Dental Insuranceunmatched
  • Detail Orientedunmatched
  • Documentationunmatched
  • Droplet Digital PCR (ddPCR)unmatched
  • Drug Developmentunmatched
  • Drug Discoveryunmatched
  • Drug Interactionsunmatched
  • FDA (Food and Drug Administration)unmatched
  • GLP (Good Laboratory Practices)unmatched
  • Health Insuranceunmatched
  • High Performance Liquid Chromatography (HPLC)unmatched
  • Identify Issuesunmatched
  • Instrumentationunmatched
  • Laboratoryunmatched
  • Laboratory Analysisunmatched
  • Laboratory Techniquesunmatched
  • Ligand Bindingunmatched
  • Liquid Chromatography-Mass Spectrometry (LC-MS)unmatched
  • Mass Spectrometryunmatched
  • Necropsyunmatched
  • Organizational Skillsunmatched
  • Pharmacodynamicsunmatched
  • Pharmacokineticsunmatched
  • Pharmacologyunmatched
  • Plasmaunmatched
  • Plasma Processingunmatched
  • Prismunmatched
  • Problem Solving Skillsunmatched
  • Quality Controlunmatched
  • Quantitative Analysisunmatched
  • Real-time PCR (qPCR)unmatched
  • Sample/Specimen Processingunmatched
  • Small Moleculesunmatched
  • Standard Operating Procedures (SOP)unmatched
  • Team Playerunmatched
  • Technical Writingunmatched
  • Time Managementunmatched
  • Training/Teachingunmatched
  • Vision Planunmatched

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