New · posted Oct 31
Eikon Therapeutics · Biotechnology
Senior Manager, Pharmacovigilance
- Jersey City, NJ
- Hybrid
- Full-time
- Manager
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 an experienced Senior Manager, Pharmacovigilance to join our team. The Senior Manager, Pharmacovigilance will be responsible for the management of safety data across our portfolio of products. The successful candidate will play a critical role in ensuring the safety of our patients by proactively monitoring and assessing adverse events, as well as working cross-functionally to ensure compliance with regulatory requirements.
This role will require a minimum of 3 day a week of onsite presence (or more as business needs require) in our Jersey City, NJ office to ensure effective management, operational excellence and high-performance delivery of clinical studies and to support the expected significant team growth & collaboration.
What you need
You are a Pharmacovigilance expert with a passion for drug discovery. You are an analytical, detail-oriented, and you have an appreciation for compliance. You’re collaborative by nature with uncompromising integrity. You’re conscientious and pay almost obsessive attention to detail, documentation and organization are second nature. You are a self-starter in spirit.
- MD with 4+ years of experience in pharmacovigilance or drug safety, with a strong understanding of pharmacovigilance regulations processes.
- Strong understanding of global regulatory requirement related to pharmacovigilance and guidelines (FDA, EMA, ICH, etc.).
- Proven technical aptitude with MS Office and Veeva Safety Database is required.
- Proven ability to lead and manage pharmacovigilance activities independently.
- Excellent communication skills and ability to collaborate effectively across multidisciplinary teams.
- Detail-oriented with strong analytical and problem-solving skills.
- Experience with safety databases and pharmacovigilance systems.
- Experience interacting with health authorities during inspections and audits.
- Experience in oncology or rare diseases is a plus.
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
- Lead and manage pharmacovigilance activities for our clinical-stage programs.
- Collaborate cross-functionally with clinical development, regulatory affairs, medical affairs, and other teams to ensure the safety of our products.
- Oversee the development and maintenance of pharmacovigilance processes and procedures.
- ICSR Management: Safety mailbox management, safety data collection, end-to-end case processing (book in, triage, data entry, query generation, quality review, evaluation, medical review including narrative writing) and reporting in compliance with applicable regional regulations and guidelines.
- Generation and distribution of (periodic) line listings to business partners.
- Contribute as needed to the preparation and review of safety sections of regulatory submissions.
- Coordinate and manage relationships with external vendors and partners involved in pharmacovigilance activities.
- Provide pharmacovigilance expertise and support for product development and lifecycle management activities.
Pay and benefits
$170,000 – $204,750 a year
Employer providedThe expected salary range for this role is $170,000 to $204,750 depending on skills, competency, and the market demand for your expertise.
401k plan with company matching
Medical, dental and vision insurance with high employer premium coverage
Mental health and wellness benefits
Generous paid time off and holidays
Enhanced parental leave
Bonus and equity compensation
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 10% above the US median for Clinical Safety & Pharmacovigilance roles at this level.
This roleEmployer provided
Manager roles in the US14 roles publishing pay
| Annual base pay | Low | Median | High |
|---|---|---|---|
| This role | $170,000 | — | $204,750 |
| All US (middle half) | $142,375 | $170,000 | $179,875 |
This role: Eikon Therapeutics's own published range. Comparisons: the base pay employers published on open Clinical Safety & Pharmacovigilance roles at the same level on Regulatory Jobs, October 31, 2026. Nothing is estimated.
Career trajectory
Where this role sits in Clinical Safety & Pharmacovigilance
The general path across 113 open Clinical Safety & Pharmacovigilance 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 30 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.
- Collaboration and leadership7
- GMP and compliance5
- Clinical trial conduct4
- Documentation and SOPs3
- Lab testing and methods2
- Regulatory submissions2
- 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.
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 Manager, Pharmacovigilance at Eikon Therapeutics
Open until filled. $170K–$205K a year, employer provided.