This is a fully remote position, open to applicants in United States.

• Share insights about a "day-in-the-life" as a specialist handling data in these areas to compile regulatory submissions.

• Outline typical tasks or challenges where AI could enhance your workflows.

• Identify and describe internal pharmaceutical systems frequently utilized for standard processes.

• Create or review reference ground-truth artifacts for evaluation, such as reports, data files, modules, etc.

• Identify and incorporate realistic sources of variance or data corruption in study data.

• Detect and rectify discrepancies in data quality.

• Over 10 years of direct DMPK experience supporting programs from discovery to IND, or direct management of 10 or more IND-reaching programs.

• Demonstrated capability to convert CRO bioanalytical data, in vitro ADME results, and in vivo PK study reports into FDA-ready IND DMPK submissions.

• Strong expertise in PK modeling, with experience in at least one PBPK platform (Simcyp, GastroPlus, or PK-Sim).

• Comprehensive ADME fluency.

• Able to work independently as the principal DMPK representative in an advisory role.

• Passionate about utilizing AI/LLM tools to assess and enhance scientific outputs.

• Competitive salary and equity.

• Full healthcare coverage; we cover 100% of premiums for you and your dependents.

• Support for growing families, including an annual new parent stipend and fertility coverage through Carrot.

• Mental health support via Rula, our in-network therapist and psychiatrist network with quick availability.

• 12 weeks of paid parental leave for maternity, paternity, and adoption.

• Pet care assistance with an annual employer-funded stipend for your furry companions.

• Commuter benefits allowing you to pay for transit and parking using pre-tax dollars.

• 401(k) company matching.

• $300 health and wellness benefit quarterly.

• Daily lunch provided when you're in the office, and dinner covered when you work late.

DMPK Consultant

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