Senior Director, Project Management

Ideaya Biosciences South San Francisco HQ Updated 24 August 2026

Job description

Non-Solicitation Policy and Notice to Agencies and Recruiters: IDEAYA's Non-Solicitation Policy strictly prohibits agencies and recruiters from any contact and communication with IDEAYA employees, managers, and leaders to submit unsolicited candidate resumes and/or to solicit business partnerships . Submission of unsolicited candidate resumes by agencies or recruiters with or without a contract in place with IDEAYA Biosciences Inc. will not create any implied obligation. Failure to comply with this policy will result in disqualification from current and future business opportunities with IDEAYA Biosciences. All recruiting and talent agency decisions are strictly managed by the internal IDEAYA Human Resources function. All communication by external agencies and recruiters must be directed to humanresources@ideayabio.com. We ask that you only email your interest once. Job Summary About IDEAYA Biosciences: IDEAYA is a precision medicine oncology company committed to the discovery, development, and commercialization of transformative therapies for cancer. Our approach integrates expertise in small-molecule drug discovery, structural biology and bioinformatics with robust internal capabilities in identifying and validating translational biomarkers to develop tailored, potentially first-in-class targeted therapies aligned to the genetic drivers of disease. We have built a deep pipeline of product candidates focused on synthetic lethality and antibody-drug conjugates, or ADCs, for molecularly defined solid tumor indications. Our mission is to bring forth the next wave of precision oncology therapies that are more selective, more effective, and deeply personalized with the goal of altering the course of disease and improving clinical outcomes for patients with cancer. When you're at IDEAYA, you will be in the midst of brilliant minds working on precision medicine therapies to help cancer patients. We are passionate and committed about being on the forefront of oncology medicine, which means we all have a high internal drive that is at the very core of every person at IDEAYA. We are inquisitive, ask deep questions, and are data-driven innovators who like to collaborate and use team work to move science forward. For more information, please see www.ideayabio.com. Location: South San Francisco, CA. Position Summary: IDEAYA is seeking a Senior Director, Project Management to join the Development team. The Senior Director, Project Management will serve as the project management lead for IDE892, providing both strategic and operational leadership across one of IDEAYA's highest-priority and most complex programs. This individual will bring scientific depth and program management rigor to a multi-arm, multi-collaboration development program spanning early combination studies through potential registrational development. The role demands a seasoned leader who can think strategically alongside the Clinical and Scientific Leads while ensuring flawless day-to-day execution across a highly matrixed, fast-moving team. This position is based in our South San Francisco headquarter offices and required to be onsite four days per week per our company policy. Reporting to: Vice President, Program & Portfolio Management Job Description What you’ll do: Strategic Program Leadership Serve as Project Manager for IDE892, owning the overall program strategy in partnership with the Clinical Lead and Head of Research Integrate scientific, clinical, regulatory, and commercial perspectives into a coherent Development Plan and Target Product Profile (TPP) Lead program-level scenario planning, portfolio prioritization discussions, and trade-off analyses for Senior Leadership and the Board Serve as a key point of contact for the Roche collaboration on IDE892, supporting Joint Steering Committee preparation and cross-company alignment Anticipate strategic inflection points, including: combination selection, indication prioritization, registrational entry. Operational Execution Own and maintain the IDE892 integrated program timeline, critical path, milestone tracking, and risk register Lead cross-functional Program Team meetings; drive decision-making, document outcomes, and ensure accountability Partner with Clinical Operations to oversee study execution across IDE892-001 cohorts, including RAS combination arms and expansion into PDAC and NSCLC Manage program budget in partnership with Finance; ensure accurate forecasting and resource alignment Coordinate cross-functional readiness for IND amendments, regulatory interactions, and data readouts Risk Management & Problem Solving Proactively identify program risks across scientific, operational, regulatory, and partnership dimensions Facilitate rapid cross-functional risk assessment and drive contingency planning Escalate critical issues to Senior Leadership with clarity and recommended paths forward External Collaboration Management Support management of the Roche collaboration, including coordination of joint program teams, data sharing, and governance meetings Coordinate with CROs and other external partners in close collaboration with Clinical Operations Communication & Reporting Prepare and help present program updates for Senior Leadership Team, Board of Directors, and external partners Ensure alignment between IDE892 program plans and broader corporate priorities and timelines Requirements: PhD in a relevant life sciences discipline (e.g., biology, pharmacology, biochemistry, or related field) required Minimum 10 years of drug development experience in the pharmaceutical or biotechnology industry, with at least 5 years in program management Demonstrated experience leading cross-functional oncology program teams through Phase 1 and Phase 2 development Strong scientific fluency in oncology — ability to engage credibly with clinical, translational, and research teams Proven ability to develop and manage integrated program plans, budgets, and risk frameworks Experience managing external partnerships or collaborations at the program level Exceptional communication and facilitation skills; proven ability to align senior, cross-functional stakeholders Experience in RAS-driven cancers (PDAC, NSCLC, CRC) or MTAP/EGFR/KRAS biology Familiarity with combination oncology development strategy, including contribution-of-components frameworks Experience supporting late-phase or registrational programs through BLA/NDA or sNDA submission Prior experience in a lean, clinical-stage biotech environment managing multiple simultaneous program arms PMP certification or equivalent program management training All employees are expected to act with integrity and in full compliance with applicable laws, regulations, and IDEAYA policies, including IDEAYA’s Code of Conduct. Employees must demonstrate good judgement and ethical behavior in all business activities, maintain patient and product safety as a top priority, and report any suspected violations of law or Company policy through appropriate channels Total Rewards Along with our inspiring mission, and highly collaborative and inclusive environment, IDEAYA offers a competitive total rewards package that reflects our pay-for-performance philosophy where employees are eligible to be considered for merit-based salary increases, company discretionary short-term ince

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