Associate Director, DMPK and Bioanalysis

Prelude Therapeutics Incorporated•Wilmington, DE

About The Position

We are seeking an experienced, hands-on Associate Director to lead the day-to-day operations of the DMPK and bioanalysis laboratory. The role oversees in-house screening and bioanalytical work, coordinates outsourced studies with contract research organizations (CROs), and ensures timely delivery of study results across a portfolio that includes small molecules, targeted protein degraders, and ADCs. The Associate Director manages, trains, and mentors staff and collaborates with colleagues in biology and chemistry.

Requirements

  • BS or MS in chemistry, biochemistry, biology, or a related field, with 10+ years of relevant experience; or a PhD in a relevant field, with 5+ years of relevant experience.
  • 2+ years of related supervisory experience in a multidisciplinary environment, with demonstrated ability to manage, train, or mentor scientists or laboratory staff.
  • Practical experience with quantitative LC-MS/MS bioanalysis, including method development and optimization, sample analysis, data review, and troubleshooting.
  • Hands-on experience with SCIEX and Waters mass spectrometry and liquid chromatography platforms.
  • Working knowledge of in vitro DMPK assays such as protein binding, microsomal stability, and CYP inhibition.
  • Experience calculating, reviewing, and interpreting PK parameters from preclinical studies.
  • Strong organization and follow-through, with the ability to manage competing priorities to meet study timelines.
  • Clear written and verbal communication skills and the ability to work effectively across scientific functions.

Nice To Haves

  • Experience supporting multiple drug modalities, such as small molecules, targeted protein degraders, and ADCs.
  • Familiarity with bioanalytical approaches used for biologics and ADCs, such as ligand-binding assays or modality-specific analytical methods.
  • Experience coordinating external CRO studies and reviewing their data and reports.

Responsibilities

  • Manage the daily operation, workload, and priorities of the DMPK and bioanalysis laboratory.
  • Oversee the conduct and LC-MS/MS analysis of in vitro assays, including plasma protein binding, microsomal stability, and CYP inhibition, as well as data processing and interpretation.
  • Oversee bioanalysis of preclinical pharmacokinetic (PK) samples for small and large molecules, including sample processing, analysis by LC-MS/MS or ELISA, and PK data processing and interpretation.
  • Ensure clear, accurate, and timely delivery of study results.
  • Coordinate outsourced in vitro and in vivo studies with domestic and international CROs, from study planning and initiation through data review and reporting.
  • Manage laboratory upkeep, troubleshoot instrument issues, and coordinate routine maintenance for LC-MS.
  • Collaborate with biology and chemistry teams to align DMPK and bioanalytical work with program needs.
  • Train, mentor, and directly manage laboratory staff, supporting their technical growth, scientific judgment, and professional development.
  • Identify opportunities to improve laboratory workflows, data quality, turnaround time, and consistency.
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