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Iambic Therapeutics, a clinical-stage AI-driven life sciences company founded in 2020, is seeking an experienced Senior Project Manager to lead cross-functional planning and execution of clinical drug development programs. Based in San Diego, this role will manage and track clinical study timelines and deliverables from study start-up through execution, working closely with all clinical development functions.
Key responsibilities include:
- Lead planning, execution, and tracking of project timelines and deliverables aligned with program milestones and corporate goals
- Support relationships with third-party vendors (CROs), overseeing scope, deliverables, timelines, and performance
- Develop, integrate, and maintain detailed project plans across development workstreams, including scenario planning, resource forecasting, risk assessments, and budget tracking
- Partner with Clinical Operations to develop, update, and track clinical study timelines and critical path activities
- Facilitate internal team meetings by creating agendas, capturing minutes and decisions, tracking action items, and ensuring follow-through
- Maintain accurate project documentation including status reports, risk registers, timelines, and meeting records
- Monitor progress against project plans and proactively identify risks, delays, or resource gaps; lead or support mitigation strategies
- Foster strong communication among Clinical Operations, Regulatory, Safety/Pharmacovigilance, Biostatistics, Data Management, CMC, and DMPK teams
The company offers competitive pay, company-paid healthcare, flexible spending accounts, voluntary life insurance, 401K matching, uncapped vacation, and operates from a state-of-the-art San Diego facility with onsite gym and dining.
REQUIREMENTS:
- Bachelor's degree in science, healthcare, or business-related discipline with 7+ years of project management experience in pharmaceutical or biotechnology industry, OR Master's degree with 5+ years of experience
- Oncology experience preferred
- Proven ability to manage timelines, cross-functional coordination, and third-party vendor relationships
- Familiarity with regulatory submission processes
- Excellent organizational, communication, and interpersonal skills with ability to work across disciplines and levels
- Proficiency in project management tools (e.g., Smartsheet, SharePoint, Confluence, or similar)
- PMP certification or formal project management training is a plus
