New · posted Oct 31
Eikon Therapeutics · Biotechnology
Senior Clinical Trial Manager, Oncology (APAC)
- Jersey City, NJ +1 more
- 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.
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 management.
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 excellence and high-performance delivery of clinical studies and to support the expected significant team growth & collaboration.
What you need
You are a talented, experienced, growth minded individual and have a passion for excellence in advancing patient care and driving strategic operating priorities to advance patient care in Oncology or other therapeutic areas.
- Post Graduate degree with 6+ years of experience or a Bachelor's degree with 8+ years of experience in a relevant field (e.g., life sciences, healthcare, or related discipline).
- Substantial experience in clinical trial management, including leadership roles.
- Require direct working experience with APAC countries, trial conduct experience in Japan and/or China, preferred.
- Strong organizational skills with meticulous attention to detail.
- Exceptional communication and leadership capabilities.
- Proficiency in Microsoft Office Suite and clinical trial management software.
- Ability to thrive in a fast-paced and evolving work environment.
- In-depth knowledge of clinical trial processes, regulations, and industry best practices, especially for APAC countries.
- Proficiency in Asian language (Chinese, Japanese, or Korean) in speaking, and require strong English skill (reading, writing, and speaking with an ability to effectively communicate with colleagues and stakeholders at all levels), highly 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
- Trial Strategy and Oversight: Develop and implement strategic plans for clinical trials, overseeing all aspects of trial execution, including planning, monitoring, and closeout.
- Oversight and coordination of local processes, clinical and ancillary supplies management, importing and exporting requirements, supplies destruction, local electronic/hard copy filing, archiving and retention. requirements (in collaboration with TMF Operations team), insurance process management.
- Team Leadership: Lead and mentor a team of clinical trial associates, coordinators, and specialists, fostering a high-performing and collaborative work environment.
- Regulatory Compliance: Ensure strict adherence to relevant regulations, protocols, and standard operating procedures (SOPs), and keep abreast of changes in regulatory requirements. Ensure that clinical studies are conducted in accordance with approved protocols, ICH-GCP and relevant country regulations and guidelines.
- Trial Documentation: Manage and maintain accurate and up-to-date trial documentation, ensuring compliance with regulatory requirements and industry standards.
- Patient Recruitment: Collaborate with recruitment teams to optimize patient recruitment strategies and ensure the timely enrollment of eligible study participants.
- Data Management: Oversee data collection, entry, and validation processes to maintain the integrity of clinical trial data.
- Cross-functional Collaboration: Foster effective communication and collaboration among cross-functional teams, including investigators, study coordinators, vendors, and other stakeholders.
- Quality Assurance: Implement and oversee quality control processes to maintain the highest standards of data accuracy and trial conduct.
- Budget and Resource Management: Manage trial budgets and allocate resources effectively to ensure trial success within financial constraints.
- Enter and update country information in clinical, regulatory, safety and finance systems.
- Contribute or lead initiatives and projects adding value to the enterprise, as required.
Pay and benefits
$143,000 – $173,250 a year
Employer providedThe expected salary range for this role is $143,000 to $173,250 depending on skills, competency, and the market demand for your expertise.
401k with company match
Medical, dental and vision insurance
Mental health and wellness benefits
Generous paid time off and holidays
Enhanced parental leave
Bonus and equity compensation
Where you'll work
Jersey City, NJ +1 moreHybridOpen in Maps (opens in a new tab)
Also posted for: Millbrae, CA
More jobs in Jersey City, NJ +1 moreEqual 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 2% below the US median for Clinical Trial Management roles at this level.
This roleEmployer provided
Manager roles in the US26 roles publishing pay
| Annual base pay | Low | Median | High |
|---|---|---|---|
| This role | $143,000 | — | $173,250 |
| All US (middle half) | $150,000 | $162,000 | $175,000 |
This role: Eikon Therapeutics's own published range. Comparisons: the base pay employers published on open Clinical Trial Management roles at the same level on Regulatory Jobs, October 31, 2026. Nothing is estimated.
Career trajectory
Where this role sits in Clinical Trial Management
The general path across 33 open Clinical Trial Management 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 34 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.
- Clinical trial conduct11
- Collaboration and leadership10
- GMP and compliance3
- Documentation and SOPs3
- Data and digital systems2
- Investigations and CAPA1
- Validation and qualification1
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 Clinical Trial Manager, Oncology (APAC) at Eikon Therapeutics
Open until filled. $143K–$173K a year, employer provided.