Full-Time

Vice President

Program and Portfolio Management

Posted on 8/4/2026

IDEAYA Biosciences

IDEAYA Biosciences

201-500 employees

Precision oncology therapies guided by biomarkers

Compensation Overview

$308k - $380k/yr

+ Discretionary short-term incentive plan + Stock option awards

South San Francisco, CA, USA

Hybrid

Four days onsite per week are required; work-from-home flexibility is available.

Master's, PharmD, PhD, MD

Category
Business & Strategy (1)
Required Skills
Veeva
Biostatistics
Risk Management

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Requirements
  • An advanced degree (PhD, PharmD, MD, or MS) in life sciences, oncology, or a related field is preferred.
  • A minimum of 12–15 years of experience in pharmaceutical or biotechnology research and development, including at least 8–10 years in project management leadership roles with direct oversight of oncology clinical development programs.
  • A proven track record of leading cross-functional teams through Investigational New Drug submissions, pivotal trial execution, and/or New Drug Application or Biologics License Application filings.
  • Expertise in oncology drug development, clinical trial design, regulatory pathways involving the Food and Drug Administration and European Medicines Agency, and International Council for Harmonisation Good Clinical Practice guidelines.
  • Strong financial acumen, including profit and loss management, budgeting, and resource optimization.
  • Demonstrated leadership in building and developing high-performing teams in a fast-paced matrix environment.
  • Experience with antibody-drug conjugates, immuno-oncology, or targeted therapies.
  • Prior experience in a small-to-mid-sized biotechnology or pharmaceutical company with portfolio complexity and limited resources.
  • Experience managing internal programs and external contract research organization and vendor partnerships.
  • Familiarity with project management software such as Smartsheet, Microsoft Project, Veeva, or equivalent project management software, and data systems including electronic data capture and clinical trial management systems.
  • Ability to balance short-term execution with long-term portfolio planning, manage multiple high-priority projects, influence senior stakeholders, distill complex project status into executive summaries, anticipate risks, implement mitigation strategies, and foster transparency, accountability, and continuous improvement.
  • Employees must act with integrity, comply with applicable laws, regulations, and company policies, maintain patient and product safety as a top priority, and report suspected violations.
Responsibilities
  • Define and execute the project management strategy for the oncology portfolio in alignment with corporate goals and therapeutic-area priorities.
  • Lead portfolio governance, including risk assessment, critical-path management, and resource allocation across multiple programs.
  • Serve as a member of the research and development leadership team, influencing pipeline prioritization, investment decisions, and go/no-go recommendations.
  • Champion operational excellence and continuous improvement across project delivery using biotechnology and pharmaceutical project-management best practices.
  • Oversee the planning, execution, and delivery of oncology programs from preclinical development through regulatory approval and commercialization.
  • Develop and maintain cross-functional integrated project plans covering timelines, budgets, resource plans, risk-mitigation strategies, and quality oversight.
  • Ensure timely achievement of program milestones and deliverables by identifying and resolving issues affecting timelines or budgets.
  • Lead resolution of escalated delivery issues and ensure robust portfolio risk management.
  • Standardize and implement project-management tools, methodologies, and templates.
  • Build, lead, and mentor a high-performing team of project managers and coordinators.
  • Develop scalable staffing models and succession plans to support portfolio growth and evolving business needs.
  • Provide coaching, performance management, and career development for direct and indirect reports.
  • Partner with Clinical Development, Regulatory Affairs, Chemistry, Manufacturing, and Controls, Biostatistics, Data Management, Medical Affairs, and Commercial teams.
  • Facilitate communication and decision-making across project teams and functional leaders.
  • Serve as the primary liaison with external partners, including contract research organizations, contract development and manufacturing organizations, and academic collaborators.
  • Oversee project budgets through regular review of costs, resources, and vendor spending.
  • Work with Finance and Business Development on proposal development, pricing strategies, and budget forecasting for new opportunities.
  • Serve as executive sponsor for key collaborations and partnerships.
  • Lead governance meetings with partners and provide senior-level program updates to the executive team and Board of Directors.
Desired Qualifications
  • An advanced degree (PhD, PharmD, MD, or MS) in life sciences, oncology, or a related field.

IDEAYA Biosciences develops targeted cancer therapies by combining translational biomarkers with small molecule drug discovery to identify and treat specific patient populations defined by molecular diagnostics. Its product work relies on identifying biomarkers that predict which patients will respond to a given therapy and then designing and optimizing small molecules that target those biology. The company differentiates itself by grounding drug discovery in biomarker-driven precision medicine—mapping patient subgroups to therapies rather than pursuing broad oncology indications—and by pursuing partnerships and licensing to fund R&D and reach commercialization. The goal is to deliver precise, biomarker-guided cancer treatments that improve outcomes for defined patient groups and bring those therapies to market through collaborations and eventual sales of approved drugs.

Company Size

201-500

Company Stage

IPO

Headquarters

San Francisco, California

Founded

2015

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Simplify Jobs

Simplify's Take

What believers are saying

  • August 4, 2026 cash reached $1.24 billion, funding operations into 2030.
  • FDA accepted darovasertib RTOR review on April 30, 2026, accelerating potential launch.
  • Servier and AstraZeneca collaborations broaden IDEAYA's commercialization optionality across uveal melanoma and DLL3 programs.

What critics are saying

  • Q2 2026 R&D hit $108.7 million while net loss widened to $112.5 million.
  • Darovasertib still faces FDA rejection or label narrowing if OS fails to mature.
  • If darovasertib misses NDA approval, IDEAYA loses its first commercial launch and valuation anchor.

What makes IDEAYA Biosciences unique

  • Darovasertib's OptimUM-02 met endpoint on April 13, 2026, in HLA-A*2:01-negative metastatic uveal melanoma.
  • IDE892 targets MTAP-deleted, KRAS G12D-mutant PDAC with Genentech's GDC-7035, announced August 2026.
  • IDEAYA pairs synthetic-lethality biology with biomarkers, small molecules, and global combination partners.

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Benefits

Health Insurance

Dental Insurance

Vision Insurance

Wellness Program

Stock Options

Employee Stock Purchase Plan

Flexible Work Hours

Growth & Insights and Company News

Headcount

6 month growth

0%

1 year growth

4%

2 year growth

-1%
Pharmacally
Aug 19th, 2026
IDEAYA and Genentech Partner to Evaluate IDE892 Plus GDC-7035 in PDAC.

IDEAYA and Genentech Partner to Evaluate IDE892 Plus GDC-7035 in PDAC. IDEAYA and Genentech will evaluate IDE892 with KRAS G12D inhibitor GDC-7035 in MTAP-deleted, KRAS G12D-mutant pancreatic cancer. M.Pharm (Reg. Affairs) IDEAYA Biosciences has entered into a clinical collaboration with Genentech, a member of the Roche Group, to evaluate IDE892, its investigational MTA-cooperative PRMT5 inhibitor, in combination with GDC-7035 (RG6620), Genentech's KRAS G12D inhibitor, in patients with pancreatic ductal adenocarcinoma (PDAC) harboring both MTAP deletion and a KRAS G12D mutation. Under the collaboration, Genentech will sponsor the clinical combination study, while IDEAYA will supply IDE892. The companies will jointly oversee the collaboration through a shared governance structure. Targeting MTAP-Deleted, KRAS G12D-Mutant PDAC. The collaboration focuses on a molecularly defined subgroup of PDAC in which MTAP deletion and KRAS G12D mutations occur together. IDEAYA estimates that these alterations co-occur in up to approximately 15% of patients with PDAC. Patients with tumors carrying both alterations currently have no approved targeted treatment options. IDEAYA stated that combining a PRMT5 inhibitor with a KRAS G12D-specific inhibitor may have the potential to produce deeper and more durable responses in this genetically defined patient population. The new combination therefore brings together two targeted investigational approaches designed to address distinct molecular features of these tumors. IDE892 development program expands. IDEAYA is currently evaluating IDE892 in a Phase 1 study of monotherapy and combination therapy in patients with MTAP-deleted advanced solid tumors (NCT07277413). The company has also initiated a Phase 1 combination cohort evaluating IDE892 with IDE397, its proprietary MAT2A inhibitor, in non-small cell lung cancer and other solid tumors. IDEAYA plans to initiate another Phase 1 combination cohort with Roche's RG6505 in MTAP-deleted, RAS-mutant PDAC during the second half of 2026. The newly announced collaboration adds GDC-7035 as an additional KRAS-directed combination partner within the broader IDE892 development program. According to IDEAYA, the company is pursuing multiple combination strategies for IDE892, including combinations with IDE397, pan-RAS inhibitors, KRAS-mutant-specific therapies, and its lead CDKN2A compound. IDE892 shows potential best-in-class characteristics. IDEAYA reported that IDE892 has approximately 1,400-fold selective MTA-PRMT5 cooperative binding compared with SAM-PRMT5 cooperative binding. The company also reported that IDE892 was designed to lack brain penetration, with the aim of maximizing its therapeutic window. These properties are intended to support the development of IDE892 in combination with other targeted therapies, including MAT2A inhibitors, pan-RAS inhibitors, KRAS-directed therapies, and CDKN2A-directed approaches. IDEAYA also reported that IDE892 has a CYP3A4 IC50 greater than 45 micromolar and did not demonstrate time-dependent inhibition across the seven major cytochrome P450 enzymes: CYP1A2, CYP2B6, CYP2C8, CYP2C9, CYP2C19, CYP2D6, and CYP3A4. The findings were based on full kinetic CYP inactivation assays. According to IDEAYA, these drug-interaction characteristics may further support the development of IDE892 as a combination partner for targeted therapies. Terms of the collaboration. Under the clinical collaboration, IDEAYA and Genentech will each retain all commercial rights to their respective compounds, including their use as monotherapies and in combination regimens. Genentech will sponsor the clinical combination study, while IDEAYA will provide IDE892. The companies will maintain joint governance over the clinical supply collaboration and conduct of the study. Clinical significance. The collaboration will evaluate IDE892 in combination with Genentech's KRAS G12D inhibitor GDC-7035 within Genentech's Phase I/II clinical program (NCT06619587), which is evaluating GDC-7035 as a single agent and in combination with other anticancer therapies in patients with KRAS G12D-mutant advanced solid tumors. The new collaboration will specifically assess the combination in patients with PDAC harboring both MTAP deletion and a KRAS G12D mutation. The agreement also expands IDEAYA's strategy of evaluating IDE892 across multiple rational combination approaches in molecularly selected cancers. Reference. About the Writer Kalyani Boharapi (LinkedIn) is a pharmacy professional and healthcare writer currently pursuing an M.Pharm in Regulatory Affairs at Dr. D. Y. Patil College of Pharmacy, with interests in pharmaceutical regulations, drug development, and healthcare innovation. She has academic exposure to dossier preparation, scientific writing, and regulatory documentation. Kalyani has also completed certification courses in Generative AI, AI in Pharma, and Bioinformatics, and actively participates in pharmaceutical conferences to stay updated with emerging trends and advancements in the healthcare and pharmaceutical industry.

Business Insider
Aug 8th, 2026
LifeSci Capital sticks to its Buy rating for IDEAYA Biosciences (IDYA).

LifeSci Capital sticks to its Buy rating for IDEAYA Biosciences (IDYA). Aug. 8, 2026, 08:35 AM LifeSci Capital analyst Charles Zhu maintained a Buy rating on IDEAYA Biosciences today and set a price target of $58.00. * Unlock powerful investing tools with TipRanks Premium to make smarter, more confident investment decisions * Subscribe to TipRanks Smart Investor Newsletter, and discover new investing opportunities with data-backed stock picks Zhu covers the Healthcare sector, focusing on stocks such as Revolution Medicines, Kura Oncology, and IDEAYA Biosciences. According to TipRanks, Zhu has an average return of 25.9% and a 63.60% success rate on recommended stocks. IDEAYA Biosciences has an analyst consensus of Strong Buy, with a price target consensus of $51.91. Based on IDEAYA Biosciences' latest earnings release for the quarter ending June 30, the company reported a quarterly revenue of $8.86 million and a GAAP net loss of $112.45 million. In comparison, last year the company had a GAAP net loss of $77.49 million Read More on IDYA:

Ideaya Biosciences
Jun 17th, 2026
IDEAYA Biosciences announces Yujiro S. Hata elected Chairman of its Board of Directors.

IDEAYA Biosciences announces Yujiro S. Hata elected Chairman of its Board of Directors. SOUTH SAN FRANCISCO, Calif., June 17, 2026 /PRNewswire/ - IDEAYA Biosciences, Inc. (NASDAQ: IDYA), a leading precision medicine oncology company, today announced that its Board of Directors has elected Yujiro S. Hata, Chairman of the Board. Mr. Hata is currently President and Chief Executive Officer, and a member of IDEAYA's Board. Terry Rosen, Ph.D., will serve as Lead Independent Director of IDEAYA's Board. "On behalf of the Board of Directors, I would like to congratulate Yujiro on this Chair appointment," said Dr. Terry Rosen, Lead Independent Director, IDEAYA Biosciences. "Since founding IDEAYA over a decade ago, Yujiro's vision, passion for the mission, and leadership have been core to the evolution of IDEAYA from an early science-driven start-up to a leading precision medicine oncology company with an extensive clinical pipeline where commercial launch preparations are underway." "I am grateful to the board for the opportunity to serve and advance IDEAYA's vision to drive forward our important cancer research and deliver breakthrough therapies for patients to address high unmet medical needs in cancer," said Yujiro S. Hata, President and Chief Executive Officer, IDEAYA Biosciences. About IDEAYA Biosciences IDEAYA is a precision medicine oncology company committed to the discovery, development, and commercialization of transformative therapies for cancer. Its 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. Ideaya Biosciences Inc. has built a deep pipeline of product candidates focused on synthetic lethality and antibody-drug conjugates, or ADCs, for molecularly defined solid tumor indications. Its 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. Forward-Looking Statements This press release contains forward-looking statements, including, but not limited to, statements related to IDEAYA's vision, strategy, mission, future growth, advancement of its research programs, development and potential commercialization of its product candidates, preparations for potential commercial launches, and the ability to deliver breakthrough therapies to patients with cancer and address unmet medical needs. Such forward-looking statements are based on management's current expectations, assumptions and beliefs and involve substantial risks and uncertainties that could cause actual results, including, but not limited to, those related to IDEAYA's clinical programs, commercial activities, and performance and/or achievements, to differ significantly and/or materially from those expressed or implied by the forward-looking statements. Such risks and uncertainties include, among others, the uncertainties inherent in the drug development process, including the process of designing and conducting preclinical and clinical trials, enrollment rates, safety outcomes, efficacy results, regulatory interactions and decisions, and the ability to translate preclinical findings into clinical benefit, manufacturing and supply risks, competition, changes in standard of care, the timing and success of commercialization efforts, the outcome of collaborations and licensing arrangements, IDEAYA's ability to successfully establish, protect and defend its intellectual property, and other matters that could affect the sufficiency of financial resources to fund operations. IDEAYA undertakes no obligation to update or revise any forward-looking statements. A further description of risks and uncertainties that could cause actual results to differ from those expressed in these forward-looking statements, as well as risks relating to the business of IDEAYA in general, are in IDEAYA's filings with the Securities and Exchange Commission, including IDEAYA's most recent Annual Report on Form 10-K and any current and periodic reports filed with the U.S. Securities and Exchange Commission. Investor and Media Contact IDEAYA Biosciences Joshua Bleharski, Ph.D. Chief Financial Officer [email protected] SOURCE IDEAYA Biosciences, Inc.

PR Newswire
Jun 15th, 2026
IDEAYA's IDE892 PRMT5 inhibitor enters phase 1/2 trial for MTAP-deleted pancreatic and lung cancers

IDEAYA Biosciences has enrolled the first patient in a Phase 1/2 clinical trial evaluating IDE892, an MTA-cooperative PRMT5 inhibitor, combined with IDE397, a MAT2A inhibitor, for MTAP-deleted pancreatic and lung cancers. MTAP deletion occurs in up to 40% of pancreatic cancers and approximately 15% of non-small cell lung cancer. IDE892 demonstrates favourable drug-like properties, including a CYP3A4 IC50 exceeding 45 micromolar and no time-dependent inhibition of major cytochrome P450s. The company's Phase 1 monotherapy escalation has cleared multiple dose cohorts without reaching maximum tolerated dose, with expansion anticipated in Q3 2026. Preclinical studies showed dual PRMT5 and MAT2A inhibition produced potent anti-tumour activity in MTAP-deleted models. IDEAYA is also collaborating with Roche to evaluate IDE892 with pan-RAS inhibitor RG6505 in pancreatic cancer.

PR Newswire
Jun 10th, 2026
IDEAYA Announces Closing of Public Offering Including Full Exercise of Underwriters' Option to Purchase Additional Shares

/PRNewswire/ -- IDEAYA Biosciences, Inc. (Nasdaq: IDYA) today announced the closing of its underwritten public offering of 7,222,225 shares of its common stock...

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