ORIC Pharmaceuticals

Independently lead analytical development and product characterization activities for one or more molecules in CMC development.Able to independently develop and optimize analytical methods to support early and late-stage development. Expected to solve challenging problems by applicati

Independently lead analytical development and product characterization activities for one or more molecules in CMC development.Able to independently develop and optimize analytical methods to support early and late-stage development. Expected to solve challenging problems by applicati

Develop and execute ORICs global pharmacovigilance strategy in alignment with corporate objectives and applicable regulatory requirementsProvide leadership for benefit-risk evaluation safety surveillance signal detection signal management and risk management across ORICs investigation

Develop and execute ORICs global pharmacovigilance strategy in alignment with corporate objectives and applicable regulatory requirementsProvide leadership for benefit-risk evaluation safety surveillance signal detection signal management and risk management across ORICs investigation

Management of outsourced and in-house research activities. Function as a subject matter expert for tech transfer/development of processes to external vendors (contract development and manufacturing organizations/contract testing organizations CDMOs/CTOs). Create and execute plans for

Management of outsourced and in-house research activities. Function as a subject matter expert for tech transfer/development of processes to external vendors (contract development and manufacturing organizations/contract testing organizations CDMOs/CTOs). Create and execute plans for

Lead the overall biostatistics strategy across all clinical development programs from early development through registration and post-marketing activities.Provide statistical leadership for the design and execution of Phase 3 clinical trials including innovative trial design and metho

Lead the overall biostatistics strategy across all clinical development programs from early development through registration and post-marketing activities.Provide statistical leadership for the design and execution of Phase 3 clinical trials including innovative trial design and metho

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