Director, Clinical Science

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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 (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  are inquisitive, ask deep questions, and are data‑driven innovators who like to collaborate and use teamwork to move science forward.

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Location:

South San Francisco, CA

IDEAYA Biosciences is seeking a South San Francisco based experienced, motivated, outgoing Clinical Scientist. Reporting to the Sr. Medical Director, Late‑Stage Clinical Development, the Director will work closely with the clinical leader providing medical and scientific expertise to one or more clinical projects.

This position is based in our South San Francisco headquarters office and is required to be onsite four days per week per our company policy.

Reporting to:
Senior Medical Director, Late-Stage Clinical Development

Typical activities may include but will not necessarily be limited to:

• With the medical monitor (MM), writing clinical development concepts and plans for molecules at all stages of development
• With the medical monitor, writing initial and or later drafts of protocol synopses, protocols and protocol amendments
• Reviewing informed consent forms and reviewing/adjudicating site‑specific ICF requests
• Partnering with the MM and Clinical Operations on site selection, start‑up and communication activities
• With the medical monitor writing or updating clinical sections of investigator brochures
• Reviewing clinical/safety sections of NDAs/MAAs
• Serving as a member of the clinical sub team
• Reviewing and interpreting data listings including safety data and serious adverse events
• Assisting the MM as an author of clinical study reports and associated publications
• Creating clinical study‑ or program‑related slide decks for internal and external use
• Training of colleagues, CRO and study site staff on the therapeutic area, molecule and protocols as appropriate
• With the MM organizing and participating in opinion leader advisory boards
• Contributing to or performing therapeutic area/indication research and competitor analysis
• With the MM support Health Authority (HA) interaction, accountable for providing responses to HA inspection observations and…