Top Healthtech Operations & Support Jobs in San Francisco, CA

The role involves coordinating the 340B Drug Pricing Program, ensuring compliance, conducting audits, and performing data analysis within the healthcare system.

Manage patient account balances, submit claims, resolve errors, ensure compliance with regulations, provide customer service, and support financial operations.

Manage patient account balances through accurate claim submissions and compliance with billing regulations, providing customer support and resolving inquiries.

The Surgery Scheduler coordinates surgical services, maintains schedules for procedures, verifies equipment availability, and documents patient information.

The Scientific Associate Director - Toxicology oversees nonclinical safety evaluations, designs toxicity studies, collaborates with regulatory agencies, and develops safety strategies for drug candidates in various diseases.

The Business Manager will facilitate governance and operational processes, ensuring effective decision-making and collaboration across teams. Responsibilities include managing board operations, communications, and resources while fostering alignment and continuous improvement in governance practices.

Instructors will deliver fitness classes, monitor exercise intensity, ensure punctuality, and communicate with management on feedback and scheduling.

The Chief of Staff will partner with executives to drive strategic initiatives, improve organizational efficiency, and enhance patient outcomes in healthcare technology.

The Senior Manager, GMP Quality oversees QA in drug development, collaborating with teams on compliance, process validation, and managing quality oversight for products.

The Chief of Staff will enhance CEO's effectiveness by managing strategic initiatives, driving operations, supporting go-to-market efforts, and facilitating cross-functional collaboration.

The Operations Associate will facilitate vertical launches, coordinate with teams, monitor internal systems, and document processes for efficiency.

The Associate Director, Study Start-Up leads feasibility activities for clinical trials and ensures efficient study start-up, collaborating across teams and optimizing processes.