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Reposted 10 Days AgoSaved
Hybrid
Emeryville, CA, USA
260K-300K Annually
Senior level
260K-300K Annually
Senior level
Biotech
The Sr. Director of Marketing Promotions will lead promotional strategies, ensure compliance with regulations, and coordinate with various departments for successful product launches and lifecycle management.
Reposted 10 Days AgoSaved
Hybrid
Emeryville, CA, USA
160K-200K Annually
Senior level
160K-200K Annually
Senior level
Biotech
The Sr. Manager / Associate Director will lead strategic forecasting and insights for Kyverna's commercial planning, ensuring data-driven decision-making and cross-functional alignment.
Top Skills: Analytics FrameworksForecasting Methodologies
17 Days AgoSaved
Hybrid
Emeryville, CA, USA
Senior level
Senior level
Biotech
The Sr. Director, Process Development leads teams to optimize and innovate cell therapy processes, ensuring compliance with regulatory standards and managing development activities for T-cell products.
Top Skills: Car-TCgmpPlasmidsProcess AutomationVectors
4 Hours AgoSaved
Remote
USA
70-90 Hourly
Mid level
70-90 Hourly
Mid level
Biotech
The Publications & Conferences Manager will oversee project management of publication deliverables and support global publication strategies and conference planning activities.
Top Skills: Medical AffairsProject ManagementScientific Communications
2 Days AgoSaved
Remote
USA
200K-235K Annually
Senior level
200K-235K Annually
Senior level
Biotech
Responsible for drafting, negotiating, and managing contracts related to clinical development in a biopharmaceutical company, ensuring alignment with company policy and regulatory frameworks.
Top Skills: Ironclad
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Reposted 4 Days AgoSaved
Remote
USA
155K-180K Annually
Senior level
155K-180K Annually
Senior level
Biotech
The Sr. Clinical Trial Manager will oversee the execution of cell therapy clinical trials, ensuring compliance, managing budgets and timelines, and coordinating with cross-functional teams.
Top Skills: BudgetingCell TherapyClinical OperationsEmaFdaIch-GcpRegulatory ComplianceSite Management
Reposted 4 Days AgoSaved
Remote
USA
250K-300K Annually
Senior level
250K-300K Annually
Senior level
Biotech
The role focuses on evaluating and advising on CAR T technologies and immune cell engineering for autoimmune diseases, conducting scientific assessments, and liaising with internal and external stakeholders.
Top Skills: AavCar TGene Delivery TechnologiesImmune Cell EngineeringLentivirusLipid NanoparticlesTargeting StrategiesVector Systems
7 Days AgoSaved
Remote
USA
Expert/Leader
Expert/Leader
Biotech
The Senior GxP Auditor leads GCP and GMP audits, ensures compliance with regulations, and develops audit strategies and processes for a growing pipeline at Kyverna Therapeutics.
Top Skills: ArgusEqms PlatformsGCPGlpGmpGpvMedidataMicrosoft Office SuiteVeeva Vault/Rim
7 Days AgoSaved
Remote
USA
270K-300K Annually
Expert/Leader
270K-300K Annually
Expert/Leader
Biotech
The Executive Director, Regulatory Affairs will lead regulatory strategy for cell therapies, overseeing submissions, health authority engagement, and team development, ensuring commercial readiness and compliance.
Top Skills: Fda RegulationsIch GuidelinesLabeling StrategyRegulatory Submissions
21 Days AgoSaved
Remote
USA
250K-290K Annually
Expert/Leader
250K-290K Annually
Expert/Leader
Biotech
The Executive Director will optimize and manage Kyverna's supply chain function, oversee supplier selection, negotiate contracts, and lead strategic sourcing efforts across multiple regions to support business growth in cell therapy.
Top Skills: Logistics ManagementPharmaceutical OperationsProcurementSupply Chain Management
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