Eikon Therapeutics Jobs

Open positions at Eikon Therapeutics, newest first. Each listing links to the company's own application page.

Open positions
15

Newest Eikon Therapeutics openings

  • Millbrae, CA · 6 days ago

    As a member of the High-Throughput Biology Team, you will play a key role in pioneering drug discovery screening assays using Eikon's proprietary live-cell, single-molecule high-throughput…

  • Jersey City, NJ · 6 days ago

    We are currently seeking an experienced, collaborative, detail oriented Manager, Study Start Up expert.

  • Jersey City, NJ · 6 days ago

    The Director Study Site Engagement & Monitoring Excellence (CONTRACT) will be responsible for leading the development and execution of Eikon's global trial site engagement strategy…

  • Jersey City, NJ · 9 days ago

    As a Clinical Trials Associate, APAC in Oncology, you will play a crucial role in supporting the planning, coordination, and execution of Phase I-III insourced global clinical studies…

  • Lab Operations Supervisor

    $95k – $105k/yr

    Millbrae, CA (On-site) · 19 days ago

    As the Lab Ops Supervisor, you will oversee day-to-day operations of our chemistry labs, supervise 1 direct report (lab support technician), directly report to the Senior Director, and…

    • Full-time
    • Lead / Staff
    • 2+ years
    • chemical inventory management
    • hazardous waste disposal (EPA/OSHA)
    • lab safety protocols
  • Jersey City, NJ · 21 days ago

    We are seeking an experienced Senior Manager, Pharmacovigilance to join our team.

    • Full-time
    • Director
    • 4+ years
    • Veeva Safety Database
    • ICSR case processing
    • global pharmacovigilance regulations (FDA, EMA, ICH)
  • Millbrae, CA · 22 days ago

    In partnership with the Director of Process Management for Clinical Research & Development, to whom this role reports, the Clinical Quality Operations Manager (CQOM) is accountable for the…

    • Full-time
    • Lead / Staff
    • GCP
    • clinical quality management
    • risk-based quality plans
  • Jersey City, NJ · 30 days ago

    We are seeking a seasoned physician with a strong clinical background and a passion for drug development to join our Clinical Development team to serve as a Study Responsible Physician as…

    • Full-time
    • Director
    • 10+ years
  • Jersey City, NJ (On-site) · 30 days ago

    As Senior Director of Translational Medicine, you will play a vital role in driving biomarker research for our innovative clinical pipeline.

    • Full-time
    • Director
    • 10+ years
    • translational medicine
    • biomarker development
    • clinical trial design
  • Jersey City, NJ · 30 days ago

    We are seeking a highly skilled and experienced Associate Director, Clinical Data Management, to provide strategic leadership and operational oversight for our data management activities.

    • Full-time
    • Director
    • 8+ years
    • clinical data management
    • EDC systems
    • regulatory compliance (GCP)
  • Jersey City, NJ (On-site) · 30 days ago

    We are seeking an experienced Director, Regulatory Affairs to support and execute regulatory strategy across our clinical-stage development programs.

    • Full-time
    • Director
    • 10+ years
    • FDA regulatory requirements
    • clinical regulatory affairs
    • IND submissions
  • Jersey City, NJ · 30 days ago

    As a Senior Clinical Trial Manager, you will play a pivotal role in leading and overseeing our global clinical trial operations.

    • Full-time
    • Director
    • ICH-GCP
    • clinical trial oversight
    • regulatory compliance
  • Jersey City, NJ · 30 days ago

    We are seeking an experienced Senior Director, Regulatory Affairs, to lead our regulatory strategy and compliance efforts.

    • Full-time
    • Director
    • 12+ years
    • FDA regulatory requirements
    • IND applications
    • NDA submissions
  • Jersey City, NJ · 30 days ago

    We are seeking a physician with a strong clinical background and a passion for drug development to join our Clinical Development team to serve as a Study Responsible Physician, Senior…

    • Full-time
    • Director
    • 5+ years
    • clinical trial design
    • medical monitoring
    • GCP
  • Jersey City, NJ · 30 days ago

    The Associate Director, Clinical Study Management, EMEA/LATAM will be responsible for overseeing the execution of clinical trials in oncology and other therapeutic areas, as required.

    • Full-time
    • Director
    • 10+ years
    • ICH-GCP
    • multi-center global clinical trials
    • Veeva TMF

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