Top Pharmaceutical Jobs in San Francisco, CA

Assist in developing and maintaining data processing pipelines, collaborating with teams to define requirements, and enhancing infrastructure for data sets.

Administer and optimize customer support tooling (Zendesk, Talkdesk, IVR, etc.), manage agent onboarding/offboarding and access, configure automations and routing, troubleshoot integrations and data discrepancies, collaborate cross-functionally to implement scalable solutions and improve support efficiency and user experience.

The Account Manager will manage employer and business partnerships, ensuring client satisfaction through effective communication and coordination across teams, overseeing account activities, and optimizing client outcomes.

The Senior Data Engineer will transform real-world data into analytics-ready datasets, build scalable pipelines, and conduct analyses to support scientific and business decisions, collaborating closely with data science teams.

The Dermatology Senior Health and Science Specialist manages business relationships, promotes products, and engages customer accounts, leveraging strong sales and product knowledge.

As a Senior Data Engineer, you will design and develop AI-powered data solutions, investigate tools, and collaborate with engineering to enhance Sleuth's platform.

The Director of Business Development drives revenue growth, strategic partnerships, and complex deal closures in the life sciences sector using SaaS solutions.

The Technical Writer creates clear, user-centric documentation for the elluminate platform, collaborating with product managers and engineers to translate complex functionalities into practical guides and resources.

The Principal Technical Project Manager ensures quality delivery of eCS services, oversees product management, develops project roadmaps, manages budgets, and fosters client relationships. They also lead teams, resolve issues, and implement process efficiencies.

The Chief Operating Officer will lead operational execution and manage delivery teams, drive company-wide operating rhythms, and partner closely with the CEO and leadership team to scale the organization and enhance operational effectiveness.

The Senior Director of Quality Assurance oversees GMP/GLP compliance, manages quality events, leads a QA team, and ensures regulatory readiness for clinical materials.

The Senior Manager, Quality Operations ensures GMP compliance in clinical development, manages quality systems, oversees manufacturing operations, conducts audits, and supports inspections.

The Director of Quality Management Systems will enhance PQMS infrastructure, lead assessments and improvements, and manage QMS teams for regulatory compliance.

The Oncology Regional Key Account Lead is responsible for executing strategies to drive demand and account management for Astellas' oncology portfolio, building relationships with key stakeholders, and enhancing access to therapies. The role involves collaboration with internal teams to develop tailored business plans and monitor performance to meet strategic goals.

The People Partner provides HR expertise, case management support, and advises management on HR policies. Responsibilities include resolving employee issues, collaborating on business changes, and delivering HR processes while maintaining compliance and promoting continuous improvement in HR services.

The Senior Executive Assistant provides communication, scheduling, and office management support to senior leaders while ensuring efficient operations and confidentiality.

The Senior Scientist in Protein Science & Engineering will lead bioanalytical research on ADCs using mass spectrometry, mentor junior staff, and support drug development and characterization projects.

The Technical Lead will build software systems for AI-native drug discovery, design data pipelines, develop APIs, and collaborate with scientists to create efficient workflows and solutions.

Oversee and manage clinical trial activities, ensuring compliance with protocols and regulations, while mentoring site staff and maintaining data integrity.

Conduct site qualification, initiation, monitoring, and close-out visits; ensure protocol compliance, data integrity, and patient safety; collaborate with investigators and site staff; perform data review and query resolution; contribute to study documentation and clinical study reports.

As a Global Study Manager, you will oversee clinical budgets, develop monitoring plans, manage study start-ups, drive enrollment, and foster relationships with stakeholders.