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Research Associate - DMPK / Bioanalysis

  • Lexington, MA, United States

$55,000 to $60,000 USD / year

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Job details

Pay
$55,000 to $60,000 USD / year
Experience
1–3 years of relevant laboratory experience in bioanalysis, analytical chemistry, DMPK, pharmaceutical research, or a related field.
Posting language
English
Posted

Original 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.
More about this job

Skills

  • Research
  • Analytical chemistry
  • Laboratory techniques
  • Pharmacology
  • Sample preparation
  • Mass spectrometry
  • Data analysis
  • Documentation
  • Quality assurance procedures
  • Attention to detail
  • Organizational skills
  • Communication skills
  • Problem solving
  • Teamwork
  • Work independently
  • Biotechnology
  • Good laboratory practices

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