New · posted Oct 31
Eikon Therapeutics · Biotechnology
Senior Director, Clinical Research (Medical Director)
- Jersey City, NJ
- Hybrid
- Full-time
- Director
The role
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.
We are seeking a physician with a strong clinical background and a passion for drug development to join our Clinical Development team to serve as a Study Responsible Physician, Senior Director, Clinical Research. In this role, you will play a pivotal part in advancing our oncology and/or non-oncology pipeline by providing medical expertise, leadership, and operational oversight for a clinical development study(ies).
What you need
You are a highly accomplished professional who excels in the development and execution of clinical projects. As a key member of the cross-functional Development Teams and the Clinical Study Teams, you will employ your expertise in clinical development to advance new therapies to patients in need. Your dedication to scientific rigor and meticulous attention to detail is evident in all your work. With a deep passion for creating important new medicines, you are committed to advancing the field of medical research and improving patient outcomes.
This role will require a minimum of 3 days a week of onsite presence (or more as business needs require) in our New Jersey office to ensure effective collaboration and high-quality execution of your clinical work.
- MD or DO degree with significant experience in Oncology.
- Minimum of 5-7 years of clinical experience, including 3+ years in drug development.
- Experience in clinical practice with direct patient care.
- Proven track record in leading clinical trials, including medical monitoring of early and late stage clinical trials.
- In-depth knowledge of clinical research methodologies, GCP, and regulatory requirements.
- Ability to work effectively in a matrixed environment.
- Strong analytical, organizational, and problem-solving skills.
- Excellent communication and interpersonal skills, with the ability to collaborate effectively with cross-functional teams.
- Passion for clinical trials and improving patient outcomes.
- Experience with IND and/or NDA/BLA filings is preferred.
At Eikon, employee compensation also includes bonus and equity compensation, in addition to several generous benefit programs, including:
- 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
- Enhanced parental leave benefit
- Daily subsidized lunch program when on-site
What you'll do
What You’ll Do in partnership with your Manager
- Design and conduct early-stage clinical development trials as needed, including, but not limited to assessing clinical safety and efficacy data, performing medical monitoring, and be responsible for other study-related clinical activities.
- Interpret reports, and prepare oral and written results of product research.
- Be proactive in fulfilling your responsibilities and pay particular attention to quality and accuracy of work as well as timeliness of deliverables.
- Collaborate closely with relevant functions within Eikon including discovery, translational and biomarker research scientists, toxicologists, clinical pharmacologists, drug safety specialists, and regulatory personnel.
- Work closely with functional partners (Clinical Science, Data Management, Clinical Operations, Biostatistics) to ensure an integrated approach to flawless execution and systematic oversight of study protocol(s) in clinical development.
- Work closely with functional partners to address protocol questions from Health Authorities and Ethics Committees in a consistent fashion.
Pay and benefits
$270,000 – $325,500 a year
Employer providedThe expected salary range for this role is $270,000 to $325,500 depending on skills, competency, and the market demand for your expertise.
401k with company matching
Medical, dental and vision insurance
Bonus and equity compensation
Generous paid time off and holidays
Enhanced parental leave
Mental health and wellness benefits
Where you'll work
Jersey City, NJHybridOpen in Maps (opens in a new tab)
More jobs in Jersey City, NJEqual opportunity, accessibility and legal noticesEikon Therapeutics's statements, word for word
Eikon is proud to be an equal opportunity employer and will consider all qualified applicants for employment.
We are currently not accepting any new third-party agencies or firms at this time. Please do not forward unsolicited agency resumes to our website, employees or Human Resources. Eikon Therapeutics will not pay fees to any third-party agency or firm associated with unsolicited resumes.
Job intelligence
The context around this role
Live data · October 31, 2026
Salary intelligence
How the pay compares
This role's midpoint is level with the US median for Clinical Development roles at this level.
This roleEmployer provided
Director roles in New Jersey9 roles publishing pay
Director roles in the US93 roles publishing pay
| Annual base pay | Low | Median | High |
|---|---|---|---|
| This role | $270,000 | — | $325,500 |
| New Jersey (middle half) | $298,000 | $306,000 | $306,000 |
| All US (middle half) | $258,000 | $298,000 | $318,500 |
This role: Eikon Therapeutics's own published range. Comparisons: the base pay employers published on open Clinical Development roles at the same level on Regulatory Jobs, October 31, 2026. Nothing is estimated.
Career trajectory
Where this role sits in Clinical Development
The general path across 116 open Clinical Development roles on Regulatory Jobs, with the titles they carry most. Not Eikon Therapeutics's own promotion track.
Skills DNA
What this role leans on
How many of the posting's 29 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.
- Clinical trial conduct8
- Collaboration and leadership5
- Lab testing and methods2
- Documentation and SOPs2
- Regulatory submissions2
- GMP and compliance1
- Data and digital systems1
Regulatory intelligence
The rules behind this role
Frameworks and standards this posting's work falls under, matched from its own words, each linked to the official source.
- ICHICH E6 good clinical practice(official source, opens in a new tab)The international standard for the conduct of clinical trials
- FDAFDA IND(official source, opens in a new tab)Investigational New Drug applications
- FDAFDA NDA(official source, opens in a new tab)New Drug Applications
- FDAFDA BLA(official source, opens in a new tab)Biologics License Applications
Company hiring pulse
Eikon Therapeutics on Regulatory Jobs
- 10
- Open roles
- 10
- Distinct roles
- 2
- Locations
By discipline
- Clinical8 80%
- Regulatory2 20%
By level
- Director6 60%
- Manager3 30%
- Associate & Specialist1 10%
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Senior Director, Clinical Research (Medical Director) at Eikon Therapeutics
Open until filled. $270K–$326K a year, employer provided.