ORIC Pharmaceuticals

Ensure compliance with all applicable local and global clinical regulations.Develop and execute a clinical QA strategic vision aligned to corporate and program goals.Serve as the senior Clinical QA representative on program and study teams.Provide hands-on leadership to develop implem

Ensure compliance with all applicable local and global clinical regulations.Develop and execute a clinical QA strategic vision aligned to corporate and program goals.Serve as the senior Clinical QA representative on program and study teams.Provide hands-on leadership to develop implem

ORIC Pharmaceuticals is seeking an experienced Senior Medical Science Liaison (Sr MSL) with relevant scientific clinical and therapeutic area expertise across prostate cancer non-small cell lung cancer (NSCLC) and potentially other tumor types. Reporting to the Head of Medical Affairs

ORIC Pharmaceuticals is seeking an experienced Senior Medical Science Liaison (Sr MSL) with relevant scientific clinical and therapeutic area expertise across prostate cancer non-small cell lung cancer (NSCLC) and potentially other tumor types. Reporting to the Head of Medical Affairs

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

The Senior Vice President/Vice President Regulatory Affairs is responsible for developing and executing global regulatory strategies aimed at the most efficient regulatory pathway for ORICs development programs. This position involves shaping and leading the long-term regulatory strat

The Senior Vice President/Vice President Regulatory Affairs is responsible for developing and executing global regulatory strategies aimed at the most efficient regulatory pathway for ORICs development programs. This position involves shaping and leading the long-term regulatory strat

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

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

Ensure compliance with all applicable local and global drug regulations.Oversee Quality CMC functions with oversight and authority over batch disposition manufacturing packaging labeling and testing activities to ensure product quality and timely release of materials and products.Prov

Ensure compliance with all applicable local and global drug regulations.Oversee Quality CMC functions with oversight and authority over batch disposition manufacturing packaging labeling and testing activities to ensure product quality and timely release of materials and products.Prov

Enterprise Applications Strategy & GovernanceDefine and execute a multi-year enterprise applications roadmap aligned with ORICs clinical and commercial growth strategy.Serve as system owner for ERP procurement T&E contract management and related enterprise platforms.Establish and enfo

Enterprise Applications Strategy & GovernanceDefine and execute a multi-year enterprise applications roadmap aligned with ORICs clinical and commercial growth strategy.Serve as system owner for ERP procurement T&E contract management and related enterprise platforms.Establish and enfo

Enterprise Applications Strategy & GovernanceDefine and execute a multi-year enterprise applications roadmap aligned with ORICs clinical and commercial growth strategy.Serve as system owner for ERP procurement T&E contract management and related enterprise platforms.Establish and enfo

Enterprise Applications Strategy & GovernanceDefine and execute a multi-year enterprise applications roadmap aligned with ORICs clinical and commercial growth strategy.Serve as system owner for ERP procurement T&E contract management and related enterprise platforms.Establish and enfo

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