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Manage end-to-end labeling operations across global markets, ensure compliance with regulatory requirements, coordinate teams, and oversee drug safety activities.

The Sr. Clinical Research Associate is responsible for site management and monitoring of clinical trials to ensure patient safety and compliance with regulations.

The Clinical Laboratory Study Manager manages clinical trial sample operations, ensures compliance, oversees data management, and liaises with various stakeholders to support biomarker evaluation.

The Manager, Data Analysis oversees centralized monitoring for clinical trials, ensuring effective RBQM systems, data analysis, and reporting while collaborating with cross-functional teams.

Lead and manage complex medical communication projects, ensuring timely delivery and high quality while facilitating communication among teams and stakeholders.

The Consultant will provide statistical expertise in meta-analysis, collaborate on evidence generation plans, and guide junior staff in a multi-disciplinary research environment.

Lead and coordinate global labeling initiatives, ensuring compliance with regulatory requirements. Manage label governance and support product lifecycle management across multiple markets.

Lead the data management team in clinical trials and medical affairs, ensuring quality data, project oversight, stakeholder engagement, and compliance with standards.

The Investigator Financial Analyst II manages budget forecasts for clinical projects, analyzes financial impacts, and collaborates with teams to ensure project financials are on target.

The Senior/Vice President, Technical will lead regulatory strategy initiatives, advise clients on product lifecycles, and represent Parexel as an industry thought leader while mentoring colleagues.