Top Pharmaceutical Strategic Operations Jobs in San Francisco, CA

The Associate Director of Field Strategy drives sales execution by providing insights, tools, and performance metrics, ensuring alignment across teams for effective brand execution and business reviews.

The Manager, Global Product Quality oversees compliance with GMP and DEA regulations for controlled substances, ensuring quality and regulatory oversight throughout the product lifecycle and collaborating with cross-functional teams.

The Senior Manager, Regulatory Ad Promo provides strategic regulatory advice on advertising and promotion, ensuring compliance with FDA regulations and business objectives, while managing advertising review processes and liaising with OPDP.

The Manager, Central Monitoring oversees centralized monitoring for clinical trials, analyzing key risk data, supporting study decisions, and driving process improvements.

The Feasibility Study Manager oversees global feasibility assessments, transforming questionnaires into surveys, verifying investigator readiness, managing survey execution, and ensuring successful project completion.

This position is for potential future opportunities in the Commercial field at Day One Biopharmaceuticals. Candidates should submit their resumes for consideration as the company grows.

The Clinical Compliance Manager will lead clinical evaluation documentation efforts, manage team resources, and ensure compliance with regulatory requirements for medical devices, while collaborating with cross-functional teams.

As a Clinical Research Associate, you'll oversee clinical trial activities, ensuring compliance with protocols and regulatory requirements, managing sites, and supporting data integrity and participant safety.

Oversee Quality Assurance and Compliance, drive global strategies, manage budgets, lead talent acquisition, and ensure regulatory compliance.

Responsible for coordinating and supporting remote site activities for clinical research projects, including recruitment, documentation, and communication with study sites.

Lead safety management activities including oversight of adverse events, safety plan development, and regulatory compliance. Manage safety databases and train specialists.

The Director of Quality Assurance oversees GCP compliance in clinical trials, manages audit programs, and leads QA teams to ensure regulatory adherence.