Crinetics Pharmaceuticals

Crinetics Pharmaceuticals is dedicated to advancing treatments for rare endocrine diseases, aiming to enhance patients' lives by developing innovative therapies

Associate Director, Pharmacometrics

DirectorDirectorFull TimeRemoteSeniorCompany Site

Location

California

Posted

26 days ago

Salary

$154K - $192K / year

Seniority

Senior

Postgraduate Degree8 yrs expEnglish

Job Description

• Support Crinetics’ translational and early clinical programs by applying mechanistic and quantitative modeling to guide decision-making • Conduct PBPK and/or QSP modeling directly and/or work with external partners to integrate preclinical, in vitro, biomarker, and early clinical data into predictions • Help identify quantitative needs at key development milestones and ensure modeling results are translated into clear, actionable insights • Contribute to scientific review and provide input on population PK, PK/PD, and exposure–response analyses performed internally or through CRO partners • Inform efficient study designs using mechanistic and empirical modeling to guide dose selection, sampling, and biomarker strategy • Draft, develop and review program‑level quantitative analysis plans • Communicate modeling results clearly to project teams, supporting decision-making and governance discussions • Contribute modeling content to regulatory submissions (e.g., INDs, NDAs, IBs) with increasing independence • Support departmental objectives, mentor junior staff as appropriate

Job Requirements

  • Pharm.D/Ph.D. or MS in Pharmacokinetics, Pharmaceutical Sciences, Pharmacology, Chemistry, Biochemistry, or related field with a strong understanding of clinical pharmacology principles
  • Significant industry experience (Associate Director: MS and 8 years of experience; PhD/PharmD with 5 years of experience) in clinical pharmacology data analysis and interpretation
  • Experience with PBPK modeling, QSP modeling, and/or integration of AI/ML into clinical pharmacology decision-making
  • Experience interpreting and overseeing population PK and exposure–response analyses
  • Familiarity with all stages of clinical drug development, including experience in the preparation of components of the Clinical Pharmacology sections of Regulatory submissions for IND- and NDA-stage projects
  • Experience working in a cross functional team and matrix environment
  • Strong written, presentation and verbal communication skills
  • Ability to influence business leaders at all levels
  • Critical thinker with strong problem-solving skills
  • Demonstrated ability to apply quantitative methods to complex problems with growing independence

Benefits

  • discretionary annual target bonus
  • stock options
  • ESPP
  • 401k match
  • top-notch health insurance plans for employees (and their families) to include medical, dental, vision and basic life insurance
  • 20 days of PTO
  • 10 paid holidays
  • winter company shutdown

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