Full-Time

Associate Director

Biomarker & Assay Development

Updated on 8/23/2026

Arbor Biotechnologies

Arbor Biotechnologies

Compensation Overview

$165k - $185k/yr

Cambridge, MA, USA

In Person

On-site presence in the Cambridge office is required, typically 4–5 days per week.

PhD

Category
Biology & Biotech (1)
Required Skills
Data Analysis
Requirements
  • A PhD or equivalent experience in biology, pharmacology, molecular biology, bioengineering, or a related field.
  • At least 8 years of relevant industry experience in biomarker development, bioanalytical assay development, translational research, or preclinical development.
  • Deep expertise in bioanalytical assay methods, development, qualification, and validation, ideally supporting genetic medicine, adeno-associated virus, RNA, or gene editing programs.
  • Experience with assay platforms and readouts such as quantitative polymerase chain reaction/digital droplet polymerase chain reaction, enzyme-linked immunosorbent assay/mesoscale discovery, flow cytometry, next-generation sequencing, biodistribution, editing efficiency, immunogenicity, RNA/protein biomarkers, or other molecular/cellular assays.
  • Experience supporting Investigational New Drug-enabling studies, Good Laboratory Practice toxicology studies, and regulatory documentation.
  • Ability to synthesize complex biomarker and assay data into clear recommendations for program teams and leadership.
  • Strong understanding of regulatory expectations for bioanalytical assays, translational biomarkers, and preclinical study packages.
  • Experience managing contract research organizations and vendors while ensuring quality, timelines, and scientific rigor.
  • Prior experience with adeno-associated virus or other genetic medicine delivery platforms.
  • Demonstrated experience managing and mentoring research associates and/or junior scientists.
  • Ability to work independently and collaboratively in a fast-paced, matrixed team environment.
  • Excellent planning, organization, communication, and interpersonal skills.
Responsibilities
  • Serve as the Biomarker and Assay Development lead on cross-functional program teams.
  • Develop and execute biomarker and bioanalytical assay strategies supporting in vivo gene editing programs from discovery through Investigational New Drug-enabling studies.
  • Design, oversee, and interpret translational and preclinical studies evaluating editing activity, target engagement and pharmacodynamic response, biodistribution, safety biomarkers, and disease-relevant endpoints.
  • Lead assay development, vendor selection, qualification, validation, transfer, and troubleshooting with internal teams and external contract research organizations and vendors.
  • Select, manage, and oversee contract research organizations to ensure high-quality and timely delivery of study results and assay data.
  • Integrate biomarker and assay data into program decision-making and regulatory documentation.
  • Collaborate with the clinical team to coordinate study-sample management, bioanalytical sample-analysis timing and cadence, quality control of assay runs, data analysis, and data presentation.
  • Manage, mentor, and develop a team of 3–4 research associates.
Desired Qualifications
  • Gene editing experience is strongly preferred.
Arbor Biotechnologies

Arbor Biotechnologies

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