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Eikon Therapeutics

Develops therapies with single-molecule tracking

Executive Director - Clinical Research, Medical Director

Biology & BiotechConfirmed live in the last 24 hours
Full-timeJersey City, NJ, USA

About the Job

Requirements

  • A minimum of 10 years of clinical experience and an MD or DO degree are required, along with significant oncology experience.
  • Significant clinical-practice experience with direct patient care is required, preferably in oncology.
  • A proven track record leading clinical trials, including medical monitoring of early- and late-stage trials, and managing complex projects is required.
  • In-depth knowledge of clinical research methodologies, Good Clinical Practice, and regulatory requirements is required.
  • Ability to work effectively in a matrixed environment is required.
  • Strong analytical, organizational, and problem-solving skills are required.
  • Ability to collaborate effectively with cross-functional teams and external partners is required.

Responsibilities

  • Design and conduct early- or late-stage clinical development trials, including assessing clinical safety and efficacy data, performing medical monitoring, and carrying out other study-related clinical activities.
  • Work closely with biomarker, discovery, and translational research scientists.
  • Provide leadership for clinical teams in a matrix environment.
  • Interpret reports, prepare oral and written product-research results, and participate in discussions of strategies within Eikon's disease areas.
  • Collaborate with Clinical Science and relevant internal functions and potential partners, including discovery, translational, and biomarker research scientists, toxicologists, clinical pharmacologists, drug safety specialists, regulatory representatives, Global Clinical Operations, and support functions.
  • Establish working relationships and collaborations with external study investigators, key opinion leaders in drug development, and external alliance partners.
  • Work with Data Management, Clinical Operations, Biostatistics, Regulatory, and other functional partners to ensure an integrated strategic approach to execution and systematic oversight of clinical-development study protocols.
  • Partner with fellow study responsible physicians and clinical scientists to develop high-quality study protocols and maintain consistent processes and standards across studies.
  • Work with functional partners to address protocol questions from health authorities and ethics committees consistently.

Desired Qualifications

  • Experience with Investigational New Drug (IND) and/or New Drug Application (NDA) filings is preferred.

About the Company

Eikon Therapeutics

Develops therapies with single-molecule tracking

Eikon Therapeutics develops medicines by studying living cells with advanced engineering and data science. Its SMT platform visualizes protein motion in real time, while AI and automated workflows analyze these movements to map molecular interactions and identify drug targets. The company blends data science, chemistry, biology, engineering, and clinical expertise to inventory dynamic cellular processes at high scale, rather than relying on static snapshots. Its goal is to create therapies that improve and extend patients’ lives by targeting dynamic protein interactions inside cells.

Company size
201-500
Company stage
IPO
Headquarters
Millbrae, CA
Founded
2019

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