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The Data Management Lead will oversee clinical trial data activities, manage project timelines, engage stakeholders, and ensure high-quality, compliant data in oncology studies.

The Principal Biostatistician provides statistical leadership in clinical trials, overseeing design, analysis, and communication of results while supporting business development.

As a Senior Regulatory Affairs Associate, you will manage regulatory processes, ensure compliance, and support product launches by collaborating with cross-functional teams and local health authorities.

The Data Management Lead oversees clinical data management for oncology trials, ensuring compliance, managing teams, and engaging with stakeholders to drive project success.

The Sr. Clinical Research Associate manages sites for clinical trials, ensuring compliance with protocols and regulations, conducting monitoring visits, and collaborating with study teams.

The Study Physician is responsible for medical oversight in clinical trials, including protocol development, risk management, and ensuring compliance with medical standards throughout the trial phases.

The Senior Clinical Research Associate oversees site management and monitoring for clinical trials, ensuring compliance with GCP, patient safety, and quality execution of studies. Responsibilities include managing operational aspects, training site personnel, addressing protocol issues, and conducting monitoring activities.

The Senior Biomarker Data Curator manages clinical specimen inventory data, supports data transfers, analyzes information, and ensures quality control in data management activities.

The Clinical Study Physician oversees clinical trial protocols, ensures high medical quality, and contributes to quality monitoring while collaborating with diverse teams.

The Senior Regulatory Affairs Consultant will ensure compliance of promotional materials with US regulations, support product launches, and provide regulatory guidance across teams.