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6 open roles read nightly from companies’ own hiring pages. Each one links to the original ad.

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  • Clinical Pharmacology Consultant

    2 weeks ago

    Entrada Therapeutics · Boston, Massachusetts, United States

    Healthcare

    We are seeking a dynamic Clinical Pharmacology Consultant who will bring extensive expertise in clinical pharmacology to our clinical stage programs. The ideal candidate will have a strong background in study design within the biotechnology or pharmaceutical industry and be…

  • Manager, Commercial Strategy Analytics

    3 weeks ago

    Entrada Therapeutics · Boston, Massachusetts, United States

    HybridManager$126.8K – $166.5K a yearData & AI

    This position will report to the Director of Business Development and Corporate Strategy and support a variety of projects for the early commercial strategy team. Example workstreams include partnership and ownership across competitive intelligence, market research, and…

  • Clinical Scientist (CONSULTANT)

    3 weeks ago

    Entrada Therapeutics · Boston, Massachusetts, United States

    SeniorHealthcare

    This individual will be highly motivated and experienced clinical researcher interested in working on all phases of clinical development. Reporting to the Executive Director, Clinical Development, this individual will provide both a strategic lens and hands on support in…

  • Associate Director, Drug Product Development & Manufacturing

    2 months ago

    Entrada Therapeutics · Boston, Massachusetts, United States

    HybridDirector$175.4K – $201.2K a yearTrades & logistics

    The Associate Director, Drug Product Development & Manufacturing, is accountable for leading drug product manufacturing activities to support Entrada’s clinical stage assets and novel pipeline programs. This role ensures successful execution of clinical manufacturing operations…

  • Associate Director, Analytical Development & Quality Control

    2 months ago

    Entrada Therapeutics · Boston, Massachusetts, United States

    HybridDirector$172K – $202K a yearOperations

    In this position you will lead late-stage AD&QC activities both internally and externally related to safety, identity, and purity of oligonucleotides programs. This work will support late-stage to commercial CMC activities for drug substances and drug products used in…

  • Director, Regulatory Writing

    2 months ago

    Entrada Therapeutics · Boston, Massachusetts, United States

    Director$220K – $249.7K a yearLegal & compliance

    The Regulatory Affairs team at Entrada is a dynamic, growing team. The Director of Regulatory Writing will coordinate and lead the efficient generation of high-quality regulatory documentation to support advancing Entrada’s pipeline, from preclinical through the clinical and…

Updated 07 Nov 2026 10:21 UTC from the OptiTalent job library.