ORIC Pharmaceuticals

Support document processing review and release of regulated GxP documents .Collaborate closely with document owners to resolve any documentation discrepancies identified during review.Organize review and support activities to ensure timely review and completion of documentation task t

Support document processing review and release of regulated GxP documents .Collaborate closely with document owners to resolve any documentation discrepancies identified during review.Organize review and support activities to ensure timely review and completion of documentation task t

We are seeking a motivated Regulatory Affairs professional to join our team and help advance the clinical development of oncology this role you will collaborate closely with colleagues across regulatory operations quality CMC nonclinical and clinical functions to support high-quality

We are seeking a motivated Regulatory Affairs professional to join our team and help advance the clinical development of oncology this role you will collaborate closely with colleagues across regulatory operations quality CMC nonclinical and clinical functions to support high-quality

Support Quality Assurance (QA) Batch Record Review Product Disposition in the review and assessment GMP manufacturing and testing records ensuring all records are complete accurate and compliant prior to product disposition.Collaborate closely with Technical Operations and/or third-pa

Support Quality Assurance (QA) Batch Record Review Product Disposition in the review and assessment GMP manufacturing and testing records ensuring all records are complete accurate and compliant prior to product disposition.Collaborate closely with Technical Operations and/or third-pa

1. Support regulatory submission and strategic direction for all ORICs development programs. 2. Lead to deliver high quality and timely regulatory submissions in alignment with corporate goals and in compliance with all applicable regulatory requirements.3. Coordinate and collaborate

1. Support regulatory submission and strategic direction for all ORICs development programs. 2. Lead to deliver high quality and timely regulatory submissions in alignment with corporate goals and in compliance with all applicable regulatory requirements.3. Coordinate and collaborate

1. End-to-End CMC Leadership & Cross-Functional IntegrationCreate and execute against integrated cross-functional project plans leading the integrated CMC strategy.Translate program strategy into cohesive development manufacturing and supply plans with clear milestones and deliverable

1. End-to-End CMC Leadership & Cross-Functional IntegrationCreate and execute against integrated cross-functional project plans leading the integrated CMC strategy.Translate program strategy into cohesive development manufacturing and supply plans with clear milestones and deliverable

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

Design planning and execution of multi-step experimental studies to provide safe efficient robust and scalable processes.Independently use PAT and analytical tools and interpret data to gain reaction understanding.Share literature and available resources to support relevant precedent

Design planning and execution of multi-step experimental studies to provide safe efficient robust and scalable processes.Independently use PAT and analytical tools and interpret data to gain reaction understanding.Share literature and available resources to support relevant precedent

Clinical and Medical LeadershipServe as the medical lead for one or more oncology programs across all phases of developmentProvide medical monitoring oversight for global clinical trials including Phase 13 and registration-enabling studies.Act as the primary medical expert for interna

Clinical and Medical LeadershipServe as the medical lead for one or more oncology programs across all phases of developmentProvide medical monitoring oversight for global clinical trials including Phase 13 and registration-enabling studies.Act as the primary medical expert for interna

1. End-to-End CMC Leadership & Cross-Functional IntegrationCreate and execute against integrated cross-functional project plans leading the integrated CMC strategy.Translate program strategy into cohesive development manufacturing and supply plans with clear milestones and deliverable

1. End-to-End CMC Leadership & Cross-Functional IntegrationCreate and execute against integrated cross-functional project plans leading the integrated CMC strategy.Translate program strategy into cohesive development manufacturing and supply plans with clear milestones and deliverable