Eikon Therapeutics Job Trends
4
Active Jobs (Last 14 Days)
0
Fresh Jobs (Last 3 Days)
100%
Jobs with Salary Data
Recent Job Posting Activity (30 Days)
Job Category Distribution
Current Eikon Therapeutics Jobs, Salary Data, and Stats
In the last two weeks, Eikon Therapeutics has posted 4 positions. None of those roles offer remote or hybrid work. We've been tracking Eikon Therapeutics since March 2, 2025.
Career Tracks Currently Hiring
Currently Hiring Office Locations
Hayward, CA New York, NY Jersey City, NJ New Jersey, NJ New York City, NY and 20 moreCurrent Eikon Therapeutics Jobs
Last updated: Feb 19, 2026
Showing 4 active jobs. Active jobs were posted in the last 14 days. Fresh jobs were posted within the last 3 days. Click a row for more details.
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| Role | |
|---|---|
Associate Director, Clinical Data Analytics and ReportingFeb 12 $191,000 - $209,000 Millbrae, CA Apply →Associate Director, Clinical Data Analytics and ReportingApply →Feb 12 $191,000 - $209,000
Millbrae, CAPosition The Associate Director, Clinical Data Analytics and Reporting is a leader responsible for establishing and scaling a Clinical Research & Development clinical analytics function for a growing biotechnology company. This role will define the analytics strategy, operating model, and technology roadmap, including the technical implementation to enable high-quality, data-driven decision-making across Clinical Research & Development, with primary focus on oncology programs.This is a hands-on role requiring demonstrated expertise in design, development, test and support of complete analytics & reporting system lifecycle. This leader will partner closely with Clinical Operations, Biostatistics, Data Management, Clinical Research, Regulatory, Safety and... | |
Clinical Trial Associate, Oncology, EMEAClinical
Feb 10 $104,000 - $114,000 Millbrae, CA; Jersey City, NJ Apply →Clinical Trial Associate, Oncology, EMEAApply →Clinical
Feb 10 $104,000 - $114,000
Millbrae, CA; Jersey City, NJPosition As a Clinical Trials Associate in Oncology, you will play a crucial role in supporting the planning, coordination, and execution of Phase I-III insourced global clinical studies within the oncology portfolio. Operating in a dynamic and collaborative environment, you will provide essential support for the execution of clinical trials, contributing to the development of groundbreaking therapies with the potential to transform patient lives. This role will require a minimum of 3 days a week of onsite presence (or more as business needs require) in either of our Jersey City (NJ) or Millbrae (CA) offices to ensure effective management, operational... | |
Senior Director, Intellectual Property (IP)Apply →Feb 9 $239,000 - $261,250
Millbrae, CAPosition We are seeking a highly experienced Senior Director of Intellectual Property (IP) to lead the development and execution of our global IP strategy in support of our mission to advance transformative therapies. Reporting to the Vice President, Intellectual Property, and based in Millbrae, CA, you will be responsible for overseeing a comprehensive IP portfolio that spans research, technology, and clinical development.In this role, you will work closely with cross-functional teams, including scientists, engineers, and clinical experts, to build and protect high-value intellectual property assets. You will provide strategic guidance on IP matters at all stages of development, ensuring alignment... | |
Clinical Trial Manager, Oncology, AsiaClinical
Feb 6 $130,000 - $142,500 Jersey City, NJ; Millbrae, CA Apply →Clinical Trial Manager, Oncology, AsiaApply →Clinical
Feb 6 $130,000 - $142,500
Jersey City, NJ; Millbrae, CAPosition We are seeking a talented, experienced, and highly motivated Clinical Trial Manager (CTM) to join our oncology Clinical Operations team. This role will require onsite presence a minimum of 3 days a week in our Millbrae, CA or Jersey City, NJ office to ensure effective global clinical trial management. The candidate must have the ability to work independently, be an effective leader, and an engaged clinical study team member in a dynamic, fast-paced environment. You will play a key role in contributing to high quality in-house clinical study management, ensuring compliance with regulatory guidelines, and contributing to planning, managing... | |