ORIC Pharmaceuticals

Global Drug Safety & Pharmacovigilance OperationsManage end-to-end pharmacovigilance activities for clinical trials and post-approval oncology productsIn partnership with Clinical Research Organizations (CROs) oversee intake assessment processing medical review and reporting of ICSRs

Global Drug Safety & Pharmacovigilance OperationsManage end-to-end pharmacovigilance activities for clinical trials and post-approval oncology productsIn partnership with Clinical Research Organizations (CROs) oversee intake assessment processing medical review and reporting of ICSRs

Independently lead analytical development and product characterization activities for our drug development portfolios. Provide oversight technical guidance and tactical direction for analytical method development transfer validation release and stability testing activities at CDMOs. F

Independently lead analytical development and product characterization activities for our drug development portfolios. Provide oversight technical guidance and tactical direction for analytical method development transfer validation release and stability testing activities at CDMOs. F

Perform sample analysis using general laboratory techniques such as weighing pipetting and operating laboratory instruments (HPLC LC-MS GC UV-Vis KF dissolution apparatus etc.).Execute analysis with a solid understanding of the test procedures underlying science and proper instrument

Perform sample analysis using general laboratory techniques such as weighing pipetting and operating laboratory instruments (HPLC LC-MS GC UV-Vis KF dissolution apparatus etc.).Execute analysis with a solid understanding of the test procedures underlying science and proper instrument

Develop and maintain a comprehensive understanding of the companys oncology pipeline R&D capabilities and strategic objectives. Lead competitive intelligence and therapeutic area landscape assessments in prostate cancer and non-small cell lung cancer providing actionable insights to

Develop and maintain a comprehensive understanding of the companys oncology pipeline R&D capabilities and strategic objectives. Lead competitive intelligence and therapeutic area landscape assessments in prostate cancer and non-small cell lung cancer providing actionable insights to

Key Responsibilities:Build and lead the Global Medical Affairs (GMA) strategy and core capabilities in areas such as medical communications operations field medical and a robust independent scientific research assessment process for all oncology assets.Align medical strategy with corp

Key Responsibilities:Build and lead the Global Medical Affairs (GMA) strategy and core capabilities in areas such as medical communications operations field medical and a robust independent scientific research assessment process for all oncology assets.Align medical strategy with corp

Key Responsibilities:Build and lead key Global Medical Affairs (GMA) capabilities in areas such as medical communications operations field medical and a robust independent scientific research assessment process.Facilitate the development and execution of the multi-year US and global m

Key Responsibilities:Build and lead key Global Medical Affairs (GMA) capabilities in areas such as medical communications operations field medical and a robust independent scientific research assessment process.Facilitate the development and execution of the multi-year US and global m

Oversee and direct all CMC regulatory strategies in compliance with global regulatory requirements for the development of ORICs products.Provide CMC regulatory support for new and ongoing clinical trials e.g. manage/prepare CMC document packages in support of INDs CTAs and amendments

Oversee and direct all CMC regulatory strategies in compliance with global regulatory requirements for the development of ORICs products.Provide CMC regulatory support for new and ongoing clinical trials e.g. manage/prepare CMC document packages in support of INDs CTAs and amendments