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Lead / Manager

Director, Site Engagement & Monitoring Excellence

Confirmed live in the last 24 hours

Eikon Therapeutics

Eikon Therapeutics

Jersey City, NJ; Millbrae, CA
On-site
Posted April 9, 2026

Job Description

Eikon Therapeutics is a new biopharmaceutical company employing revolutionary technology at the intersection of chemistry, engineering, computation, and biology to discover novel treatments for life-threatening diseases. Eikon’s discovery platform is built on groundbreaking innovations from its founders (Nobel Prize, 2014), culminating in the creation of microscopes which enable real time, molecular-resolution measurements of protein movement in living cells, thereby unlocking otherwise intractable classes of proteins as drug targets.

Position

The Director Study Site Engagement & Monitoring Excellence will be responsible for leading the development and execution of Eikon’s global trial site engagement strategy, including oversight and accountability for all internal/external managed site monitoring activities to ensure predictable delivery of high-quality data and establish Eikon as a preferred sponsor for clinical sites.

The Director will ensure effective collaboration with clinical study teams, and Functional Service Provider (FSP) partners, to implement excellent site relationship management and site monitoring activities to accelerate operational excellent delivery of Eikon’s clinical programs.

This role will require a minimum of 3 days a week of onsite presence (or more as business needs require) in either of our California or New Jersey offices to ensure effective management, operational excellence and high-performance delivery of clinical studies and to support the expected significant team growth & collaboration.

What You’ll Do

Strategic Leadership

  • Define and implement site engagement strategies to improve relationships
  • Support the build of new partnerships and networks
  • Support high quality monitoring approaches and ensure alignment with regulatory standards
  • Serve as liaison between clinical study teams and investigative sites

Operational Support

  • Provide guidance, oversight and training to the study site engagement team, including CRA site monitors, whether insourced or outsourced suppliers, to maximize effectiveness and acceleration in Eikon’s operational execution of clinical research.
  • Develop and maintain appropriate performance standards, processes and documentation for harmonized site engagement and monitoring support across Eikon’s clinical programs.
  • Maintain regular information exchange within the study site engagement team, identify common elements of stud
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