Eikon Therapeutics Job Trends
2
Active Jobs (Last 14 Days)
1
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 2 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 24 moreCurrent Eikon Therapeutics Jobs
Last updated: Aug 7, 2026
Showing 2 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 | |
|---|---|
Senior Clinical Trial Manager, OncologyFresh
Clinical
Aug 5 $143,000 - $173,250 Millbrae, CA; Jersey City, NJ Apply →Senior Clinical Trial Manager, OncologyApply →Fresh
Clinical
Aug 5 $143,000 - $173,250
Millbrae, CA; Jersey City, NJPosition As a Senior Clinical Trial Manager, you will play a pivotal role in leading and overseeing our global clinical trial operations. Operating in a dynamic and collaborative environment, you will provide strategic direction and hands-on management to ensure the successful execution of global clinical trials in multiple regions, contributing to the development of groundbreaking therapies with the potential to transform patient lives. The successful candidate will need minimal oversight, will work closely with cross-functional teams to ensure successful completion of studies within timelines and budget, with a focus on exquisite quality to support excellence and world class clinical study... | |
Senior Scientist, Analytical CMCApply →Research
Aug 4 $154,000 - $185,850
Millbrae, CAPosition Overview The Senior Scientist, CMC Analytical Lead provides analytical leadership for assigned drug substance and drug product programs from IND-enabling studies through clinical development, registration, and commercial readiness. This role supports phase-appropriate analytical strategy and execution across key CMC activities, including IND-enabling, toxicology, early through late-stage clinical supply, drug substance process development, formulation and drug product development, and manufacturing. Responsibilities include analytical input to method readiness, transfer and validation strategy, release and stability strategy, shelf-life planning, specifications, data interpretation, and regulatory submissions. This role is part of the CMC Analytical group and works closely with CMC, Quality, Regulatory, Supply... | |