New · posted Oct 31
Eikon Therapeutics · Biotechnology
Associate Director, Clinical Data Management
- Jersey City, NJ +1 more
- 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 highly skilled and experienced Associate Director, Clinical Data Management, to provide strategic leadership and operational oversight for our data management activities. As an Associate Director, you will play a pivotal role in driving the planning, execution, and quality assurance of clinical data management processes, ensuring the integrity, accuracy, and compliance of data throughout the research lifecycle. This role requires a minimum of 3 days per week onsite (or more, as business needs require) in either our Jersey City (NJ), or Millbrae (CA) offices.
What you need
You have extensive expertise in clinical data management, including data collection, database design, and quality assurance, along with a deep understanding of industry-specific data management practices. You also have technical proficiency in data management tools and software, comprehensive knowledge of regulatory guidelines, strong leadership skills, analytical acumen, and excellent interpersonal and communication abilities to collaborate effectively with cross-functional teams and partners.
- Post Graduate degree with 8+ years of relevant experience or a Bachelor’s degree with 10+ years of relevant experience in a field such as Life Sciences, Biostatistics, Computer Science, or a related discipline.
- Data Management Expertise: Extensive experience in clinical data management, including data collection, database design, and quality assurance.
- Industry Knowledge: In-depth understanding of the biotechnology or pharmaceutical industry and its data management practices, particularly within clinical research.
- Technical Proficiency: Proficiency in relevant data management tools and software, including electronic data capture (EDC) systems and data coding standards.
- Regulatory Acumen: Thorough knowledge of regulatory guidelines related to clinical data management and data integrity.
- Leadership Experience: Demonstrated leadership skills and experience in guiding and mentoring data management teams.
- Analytical Skills: Strong analytical and problem-solving skills, with the ability to address data-related challenges effectively.
- Collaborative Approach: Excellent interpersonal and communication skills to collaborate seamlessly with cross-functional teams and external partners.
- Oncology experience preferred.
- Veeva EDC experience 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
- Leadership and Strategy: Provide strategic direction and leadership for the clinical data management team, ensuring alignment with company objectives and industry best practices.
- Data Management Planning: Collaborate with cross-functional teams to develop and implement data collection strategies, tools, and systems that meet study goals and regulatory requirements.
- Quality Control: Oversee data quality control processes, including validation, discrepancy management, and reconciliation, to ensure the accuracy and completeness of collected data.
- Database Management: Lead the design and maintenance of electronic data capture (EDC) systems or databases, ensuring their efficiency and capability to capture essential data elements.
- Data Standards and Compliance: Ensure adherence to data standards, industry best practices, and relevant guidelines throughout the data management lifecycle.
- Team Collaboration: Work closely with cross-functional teams, including biostatisticians, clinical researchers, and regulatory experts, to facilitate seamless data integration and analysis.
- Regulatory Adherence: Ensure that all data management activities are conducted in full compliance with applicable regulatory standards and guidelines.
- Documentation: Maintain accurate and comprehensive documentation of data management processes, decisions, and workflows.
- Problem-Solving: Identify and address complex data management challenges proactively, proposing effective solutions to enhance data quality and operational efficiency.
- Team Development: Mentor and develop data management team members, fostering their professional growth and ensuring a high level of performance.
Pay and benefits
$178,000 – $215,250 a year
Employer providedThe expected salary range for this role is $178,000 to $215,250 depending on skills, competency, and the market demand for your expertise.
401k plan with company matching
Medical, dental and vision insurance with high employer-paid premiums
Mental health and wellness benefits
Generous paid time off and holiday policies
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 level with the US median for Clinical Data Management roles at this level.
This roleEmployer provided
Director roles in the US6 roles publishing pay
| Annual base pay | Low | Median | High |
|---|---|---|---|
| This role | $178,000 | — | $215,250 |
| All US (middle half) | $179,500 | $196,250 | $225,000 |
This role: Eikon Therapeutics's own published range. Comparisons: the base pay employers published on open Clinical Data Management roles at the same level on Regulatory Jobs, October 31, 2026. Nothing is estimated.
Career trajectory
Where this role sits in Clinical Data Management
The general path across 29 open Clinical Data 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 32 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.
- Data and digital systems17
- Collaboration and leadership9
- Clinical trial conduct5
- GMP and compliance3
- Lab testing and methods2
- Documentation and SOPs1
- 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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Associate Director, Clinical Data Management at Eikon Therapeutics
Open until filled. $178K–$215K a year, employer provided.