Director, DMPK

Evommune, Inc.; Palo Alto (CA); Hybrid; USD 190,000 - 240,000; Full time

Benefits offered by this job

Health, dental, and vision plans

401(k) plan

Paid parental leave

Employee referral bonus program

Job summary

A biotechnology company located in Palo Alto, CA, is seeking a Director of DMPK to lead scientific and strategic efforts for their small-molecule pipeline. The ideal candidate will have a PhD and over 10 years of DMPK experience, overseeing strategies that impact candidate selection and IND-enabling activities. This hybrid role includes working in the office two days per week and offers a competitive salary range of $190,000-$240,000 along with additional bonuses and benefits.

Qualifications

• 10+ years of small-molecule DMPK experience within the pharmaceutical or biotechnology industry.
• Deep expertise in ADME, PK, and PK-PD with experience translating preclinical data to clinical development.
• Experience with clinical candidate selection and first-in-human dose projections.

Responsibilities

• Provide scientific and technical leadership for DMPK, PK, and PK-PD strategy.
• Serve as DMPK program lead, with accountability for study design, execution, interpretation, and reporting.
• Develop and implement DMPK strategies aligned with project objectives.

Skills

DMPK strategy

ADME

PK and PK-PD modeling

Regulatory guidelines

Analytical skills

Education

PhD in pharmacokinetics or related discipline

Tools

Modeling and analysis tools

Job description

Evommune, Inc. (NYSE: EVMN) is a clinical‑stage biotechnology company focused on developing innovative therapies for immune‑mediated inflammatory diseases. Headquartered in Palo Alto, California, with additional operations in New York, NY, Evommune is advancing a differentiated pipeline designed to address the underlying drivers of disease.

Our scientific approach integrates deep immunology expertise with disciplined clinical development to deliver potentially best‑in‑class therapies for patients with significant unmet medical needs. For more information, visit www.Evommune.com.

Work Location:

This hybrid position is expected to be in the office two days per week, with the option to work remotely up to three days per week. Occasional additional onsite presence may be required based on business needs or operational priorities.

Our Core Values

Before we dive into the specifics of the role, it's important to highlight the core values that are integral to being a member of the Evommune team. Our values are not just words; they shape our culture, guide our decision‑making, and define what it means to be part of our team.

• Together We Win: We champion teamwork, celebrating every achievement as a shared success.
• Guided by Insight: We make data‑driven decisions, using our collective experience to shape the future of our business.
• Every Day Matters: We act with urgency to bring transformative therapies to patients by being nimble, decisive, and effective.
• Driven By Excellence: We set a high bar and hold ourselves accountable to deliver exceptional results in everything we do.
• Empowered To Act: We invest in our team and value transparency, fostering trust and a sense of ownership.

The Position

Evommune is hiring a Director, DMPK to provide scientific and strategic leadership across discovery and development programs. This role is critical to advancing our small‑molecule pipeline from early discovery through clinical development. The Director, DMPK will serve as the DMPK program lead, responsible for establishing and executing ADME, PK, and PK‑PD strategies that inform candidate selection, IND‑enabling activities, and first‑in‑human dose projections. As a subject‑matter expert, this individual will partner closely with cross‑functional teams to enable data‑driven decision‑making and efficient program execution. This role reports to the Executive Director, Non‑Clinical Development and offers the opportunity to play a visible, influential role in shaping Evommune’s growing pipeline.

Key Responsibilities

• Provide scientific and technical leadership for DMPK, PK, and PK‑PD strategy across discovery and development programs
• Serve as DMPK program lead, with accountability for study design, execution, interpretation, and reporting
• Develop and implement DMPK strategies aligned with project and portfolio objectives, including candidate selection and first‑in‑human dose predictions.
• Partner closely with Medicinal Chemistry, Pharmacology, Toxicology, CMC, Bioanalytical, and Clinical teams to support integrated program advancement
• Oversee the design, analysis, and execution of in vivo and in vitro DMPK studies, ensuring timely communication of results to project teams and senior leadership
• Provide expert interpretation of DMPK data and present findings to internal stakeholders and external partners
• Author and/or oversee PK and DMPK sections of regulatory submissions (IND, IB, CTA, IMPD, NDA/BLA) and support regulatory interactions
• Manage and collaborate with CROs, consultants, and external partners to ensure high‑quality execution and efficient use of resources
• Ensure scientific rigor, data integrity, and appropriate documentation across all DMPK activities
• Support the continued evolution and scaling of DMPK capabilities as the pipeline grows

Qualifications

• PhD in pharmacokinetics, drug metabolism, or a related discipline
• 10+ years of small‑molecule DMPK experience within the pharmaceutical or biotechnology industry
• Proven track record of leading DMPK strategy for discovery and development programs
• Deep expertise in ADME, PK, and PK‑PD with experience translating preclinical data to clinical development
• Experience with clinical candidate selection and first‑in‑human dose projections
• Hands‑on experience analyzing PK and PK‑PD data using relevant modeling and analysis tools
• Experience guiding the development and validation of bioanalytical methods for quantifying drug candidates and metabolites
• Strong understanding of regulatory guidelines supporting small‑molecule development, including preparation and review of DMPK sections for regulatory submissions
• Experience supporting or leading interactions with U.S. and international regulatory agencies
• Demonstrated ability to influence program strategy and decision‑making through DMPK insight

How You Will Lead

• Act as a trusted, influential partner to senior scientific and development leadership
• Drive the DMPK agenda with strategic thinking, scientific rigor, and a bias toward action
• Communicate complex data clearly and effectively to diverse audiences
• Operate effectively in a fast‑paced, resource‑constrained, startup environment
• Bring a collaborative, hands‑on leadership style with strong problem‑solving and analytical skills

Compensation

The salary range for this position is $190,000-$240,000, and the position may be eligible for performance‑based bonuses and/or equity‑linked compensation. Salary ranges are determined by role, level, and location, as well as additional factors such as job‑related skills, experience, and relevant education or training. We offer company‑sponsored benefits, including comprehensive health, dental, and vision plans, as well as pet insurance. In addition, we offer a 401(k) plan, ample time‑off programs, paid parental leave, life insurance, disability insurance, and an employee referral bonus program.

Evommune is proud to be an equal opportunity employer and will consider all qualified applicants for employment.