Associate Director, Clinical Regulatory
Eikon Therapeutics · Jersey City, NJ
Posted 12 days ago · $178,000 to $215,250
or apply directly on Eikon Therapeutics's site. We never take the application ourselves.
Is this posting real?
- This role has been open
- 12 days Eikon Therapeutics's roles stay open a median of 44 days
- Reposted
- No
- Salary listed
- Yes 79% of Eikon Therapeutics's roles list one
- Ghost-job risk at Eikon Therapeutics
- high 12 stale, 1 reposted of 24 open
- Hiring momentum
- 31 roles opened in the last 90 days ↑ up vs. the prior 90 days
- Last confirmed on the employer's board
- 2026-09-17
Measured from postings appearing on and disappearing from Eikon Therapeutics's own greenhouse board since 2026-08-03. Full hiring picture for Eikon Therapeutics.
About this role
The Associate Director, Clinical Regulatory at Eikon Therapeutics will manage regulatory clinical trial applications and ensure compliance with relevant regulations. This role involves developing ex-US submission strategies, collaborating with cross-functional teams, and liaising with regulatory agencies. The position requires a minimum of three days a week onsite in Jersey City, NJ, to facilitate effective management and collaboration.
- benefits
- 4/5
- freshness
- 4/5
- career value
- 4/5
- role clarity
- 5/5
- pay transparency
- 5/5
Scored from the posting itself — how clearly the role is described, how much it says about pay and benefits, and how recently it was listed. Not a judgement of Eikon Therapeutics as an employer.
What you need
- 10+ years of relevant experience with a Bachelor's degree, or 8+ years with a post graduate degree in a relevant scientific discipline
- In-depth knowledge of international regulatory requirements and guidelines
- Exceptional communication, negotiation, and project management skills
- Proven ability to thrive in a collaborative, cross-functional team environment
- Strong analytical skills, attention to detail, and effective problem-solving abilities
- Adaptability and the ability to excel in a fast-paced, high-growth environment
Nice to have
- Ability to interface well with submission platforms such as Clinical Trials Information System (CTIS) or Integrated Regulatory Information System (IRIS)
- Familiarity with study and GMP documentation required by Health Authorities
What you get
- 401k plan with company matching
- Medical (premiums covered by Eikon at 95%), dental and vision insurance (premiums covered by Eikon at 100%)
- Mental health and wellness benefits
- Weeklong summer and winter holiday shutdowns
- Generous paid time off and holiday policies
- Life/AD&D Insurance (premiums covered by Eikon at 100%) and optional supplemental employee-paid life/AD&D policies
Worth weighing
- Minimum of three days a week onsite presence required
- Role involves managing complex regulatory submissions across multiple international jurisdictions
- High level of experience required may limit applicants
- No salary listed beyond the expected range of $178,000 to $215,250
Summarised from Eikon Therapeutics's posting. Read the full original.
Listed by Eikon Therapeutics on their greenhouse job board, last confirmed open on 2026-09-17. PitchMeAI is not the employer.
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