Top Tech Jobs & Startup Jobs in Boston, MA

Lead computational analysis of deep sequencing datasets (RNA-seq, ribosome profiling, CLIP-seq, SHAPE-seq, etc.), develop pipelines, interpret results in RNA biology and disease contexts, collaborate with experimental teams, present findings, and contribute to publications, patents, and strategy for genetic medicine programs.

Provide scientific and strategic leadership for AI/ML-driven RNA therapeutics discovery. Define modeling platforms, integrate large-scale datasets (in vitro, in vivo, ADME/Tox, NGS), enable closed-loop automated DMTA cycles, mentor computational scientists, and partner across functions to deploy scalable AI/ML solutions that accelerate molecule discovery.

The role involves developing and optimizing analytical methods, providing technical oversight for assays, conducting testing and characterizations, and training team members in a collaborative environment.

Develop and implement QSP models for drug discovery and development, analyze data, communicate findings, and enhance QSP practices at Lilly.

The Principal Engineer will develop AI tools for scientific authoring, enhance document workflows, and collaborate with scientists for AI integration in regulatory and manuscript submissions.

The Associate Director will develop regulatory strategies, manage regulatory submissions, and ensure compliance with health authority standards in CMC activities.

The role requires engineering integrative solutions between AI and lab systems to enhance molecule discovery through automation and data connectivity. It involves prototyping, collaboration with scientists, deploying intelligent systems, and ensuring reliable lab operations.

The role focuses on performing potency testing and quality control processes in a GMP environment, managing analytical methods, and supporting clinical studies of gene editing medicines.

The Director leads clinical pharmacology and translational modeling strategies for gene editing therapeutics, overseeing all stages from preclinical to regulatory submission.

Develop, optimize, and validate analytical methods for gRNA, mRNA, and LNP products; coordinate method transfer with QC/CMOs; interpret and present data; author technical documents; provide technical oversight, troubleshoot assays, and mentor junior staff while collaborating cross-functionally.