ORIC Pharmaceuticals

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

 IT Business Partnership & StrategyServe as the primary IT partner for Phase 3 Development functions aligning technology solutions with business needs.Collaborate with Clinical Safety Regulatory Portfolio & Project Management and other Development functions and teams to support digita

 IT Business Partnership & StrategyServe as the primary IT partner for Phase 3 Development functions aligning technology solutions with business needs.Collaborate with Clinical Safety Regulatory Portfolio & Project Management and other Development functions and teams to support digita

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

We are seeking a highly skilled and motivated Contract Research Associate with expertise in formulation to join ORICs Discovery team. The successful candidate will support ORICs existing drug discovery programs. Also this person will play a key role in impacting the drug discovery pro

We are seeking a highly skilled and motivated Contract Research Associate with expertise in formulation to join ORICs Discovery team. The successful candidate will support ORICs existing drug discovery programs. Also this person will play a key role in impacting the drug discovery pro

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