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Senior Director/Executive Director, DMPK

Iambic Therapeutics - San Diego HQ, San Diego, California, United States

Posted May 13, 2026

Benefits

Parental leave
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Non-birth-parent leave
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Family-building benefits
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  • Adoption assistance: Not verified
  • Surrogacy assistance: Not verified
Mental health support
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Relocation assistance
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Childcare support
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Learning budget
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Verification
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Salary
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401(k) match
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Market context

U.S. role benchmark (BLS OEWS)
$81,444 U.S. median for this role
Projected growth (BLS Employment Projections)
+6.9% - Faster than average

Matched to SOC 29-1141 - Healthcare aggregate by role bucket.

Source: U.S. Bureau of Labor Statistics, OEWS, May 2024 and Employment Projections, 2024-2034.

Role

Role function
Healthcare From the posting source checked Jun 20, 2026
Seniority
Director Plus From the posting source checked Jun 20, 2026

Schedule

Shift type
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Weekend work
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Company

Company stage
Clinical-stage From the posting source checked Jun 20, 2026

Application

Cover letter
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Assessment
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Deadline
Not stated

Where they hire

State eligibility is not yet verified.

About this role

Senior Director/Executive Director, DMPK San Diego HQ, San Diego, California, United States JOB SUMMARY Iambic Therapeutics is seeking an experienced DMPK leader to lead our Drug Metabolism & Pharmacokinetics function. Reporting to senior leadership, you will define the scientific strategy for DMPK from early discovery through IND-enabling studies. You will collaborate with internal and external partners to plan and execute DMPK studies. This is a high-impact, hands-on leadership role for someone who thrives at the intersection of rigorous science and strategic drug development. KEY RESPONSIBILITIES - Lead and manage all DMPK strategy and execution across Iambic's discovery programs, setting clear goals and ensuring alignment with cross-functional program teams. - Design and oversee non-clinical ADME/PK studies and PK/PD modeling to enable candidate selection and accelerate IND filings. - Serve as the internal DMPK subject matter expert, partnering with medicinal chemistry, biology, toxicology, and clinical teams to interpret data and guide program decisions. - Build and manage a high-performing network of CRO partners and academic collaborators to supplement internal capabilities. - Lead preparation and review of DMPK sections for regulatory submissions including INDs and NDAs; interact with health authorities as needed. - Champion compliance with ICH guidelines, FDA regulations, and industry best practices across all DMPK activities. - Contribute scientific expertise to business development, due diligence, and partnership evaluations. - Stay at the forefront of emerging DMPK science, technologies, and regulatory trends to continuously strengthen the function. QUALIFICATIONS - PhD in Pharmacokinetics, Pharmaceutical Sciences, or closely related discipline or PharmD - 12+

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