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Iambic Therapeutics
Iambic Therapeutics
51 – 200 Angajați
Asistență medicalăConsultanțăIndustria prelucrătoare
Iambic Therapeutics este o companie de biotehnologie care dezvoltă abordări bazate pe inteligență artificială pentru descoperirea medicamentelor. Platforma sa combină algoritmi avansați cu experimente de mare randament pentru a explora spații chimice, a optimiza molecule pentru ținte terapeutice, a identifica mecanisme noi și a genera candidați promițători la medicamente mai eficient decât metodele convenționale de descoperire.
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Locurile de muncă ale companiei

Senior Clinical Development Project Manager - San Diego, CA Onsite

Lead cross-functional clinical drug development programs at Iambic Therapeutics, coordinating study timelines, vendors, risks, and deliverables for AI-driven medicines.

USStatele Unite ale AmericiiCACalifornia
152.000 $ – 190.000 $ / an
La sediuNormă întreagăSeniorLimbă Obligatorie: englezăOperațiuni clinice
PMP

Descriere

  • Coordinate project planning, execution, timelines, and deliverables against program milestones and corporate objectives.
  • Oversee third-party vendors, including scope, deliverables, schedules, and performance.
  • Build, integrate, and maintain detailed plans across development workstreams.
  • Conduct scenario planning, resource forecasting, risk assessments, and budget monitoring.
  • Work with Clinical Operations to manage study timelines and critical-path activities from start-up through execution.
  • Run internal meetings by preparing agendas, documenting decisions, tracking actions, and ensuring follow-through.
  • Maintain status reports, risk registers, timelines, meeting records, and other project documentation.
  • Track progress, flag risks, delays, and resource shortfalls, and support mitigation planning.
  • Coordinate communication across Clinical Operations, Regulatory, Safety/Pharmacovigilance, Biostatistics, Data Management, CMC, and DMPK.

Cerințe

  • Bachelor’s degree in a science, healthcare, or business-related field plus 7+ years of pharmaceutical or biotechnology project management experience, or a master’s degree plus 5+ years of experience.
  • Oncology experience is preferred.
  • Demonstrated ability to manage timelines, coordinate cross-functional teams, and oversee external vendors.
  • Working knowledge of regulatory submission processes.
  • Strong organizational, communication, and interpersonal skills for working across disciplines and organizational levels.
  • Experience with Smartsheet, SharePoint, Confluence, or comparable project management tools.
  • PMP certification or formal project management training is preferred but not required.
  • Must be authorized to work in the United States and live in San Diego or be willing to relocate.
  • benefits

Beneficii

  • Healthcare coverage paid by the company.
  • Flexible spending accounts.
  • Voluntary life insurance.
  • 401(k) matching.
  • Unlimited vacation.
  • Onsite gym.
  • Onsite dining.
  • State-of-the-art workplace.
  • Convenient access to places to live and enjoy.

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