Jobs at Crinetics Pharmaceuticals

The Director of Omnichannel Marketing develops and executes integrated strategies across channels to engage patients and professionals, ensuring compliance and optimizing marketing efforts through data-driven insights.

Lead pricing operations and government price reporting for Market Access. Manage AMP/Best Price/340B/NFAMP reporting, gross-to-net forecasting, rebate validation, vendor collaboration, SOPs, and cross-functional communication to support pricing, contracting, and reimbursement strategies.

Lead development and execution of global primary and secondary market research to inform commercial strategy for Palsonify and pipeline programs. Partner cross-functionally to design studies, manage vendors, generate data-driven insights, and present findings to senior leadership to support brand planning, market access, and commercialization.

Lead outsourced bioanalysis and biomarker activities including assay selection, development, validation, and CRO/CLIA lab management. Define biomarker strategies for nonclinical and clinical studies, ensure regulatory-compliant fit-for-purpose validations, oversee vendor contracts/budgets, contribute to regulatory submissions (IB/IND/NDA), and support cross-functional study goals.

Lead drafting, review, negotiation, and administration of commercial and G&A contracts. Partner with Commercial, Medical Affairs, Finance, and Compliance to improve CLM processes, templates, and workflows. Oversee contract execution, provide stakeholder guidance, manage intake and recordkeeping, and support CLM system design and training.

The Associate Director, Quality Assurance oversees GCP QA operations, conducts audits, supports clinical study activities, and ensures compliance with GCP regulations.

The Director, Global Product Leader oversees product development programs, manages cross-functional teams, and ensures strategic alignment for regulatory and commercial processes in the pharmaceutical industry.

Lead execution and administration of GMP Quality Risk Management across development, tech transfer, validation, and manufacturing. Facilitate cross-functional risk assessments (FMEA, risk ranking), maintain risk registers and QMS documentation, drive inspection readiness, KPIs, continuous improvement, and mentor junior staff while integrating QRM with CAPA, change control, and deviations.