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Reposted 19 Days AgoSaved
Remote
US
163K-213K Annually
Senior level
163K-213K Annually
Senior level
Biotech
Lead the Central Statistical Monitoring team, ensuring subject safety and data integrity in clinical trials through statistical analysis and collaboration with various stakeholders.
Top Skills: MS OfficePower BI
Reposted 19 Days AgoSaved
Remote
US
27-30 Hourly
Internship
27-30 Hourly
Internship
Biotech
The intern will support analytical development and QC activities, conduct data analysis, and manage QC documents in a fast-paced, collaborative environment.
Top Skills: MS OfficeVeeva
Reposted 19 Days AgoSaved
Remote
US
176K-236K Annually
Expert/Leader
176K-236K Annually
Expert/Leader
Biotech
The Director, Global Regulatory Project Management leads oncology regulatory strategies, ensuring successful global drug submissions, while driving operational excellence and collaboration across teams.
Top Skills: Electronic Document Management SystemsMicrosoft Office SuiteMs ProjectPower BIRegulatory Submission PlatformsSmartsheets
Reposted 19 Days AgoSaved
Remote
US
27-27 Hourly
Internship
27-27 Hourly
Internship
Biotech
The intern will assist the QMS team in document review, authorship, compliance, and change control activities, ensuring document clarity and adherence to guidelines.
Top Skills: MS Office
Reposted 19 Days AgoSaved
Remote
US
187K-247K Annually
Senior level
187K-247K Annually
Senior level
Biotech
Lead the Central Statistical Monitoring team to oversee statistical design and governance in clinical trials, ensuring data integrity and safety. Develop monitoring indicators, validate models, and communicate findings to cross-functional teams. Provide training and support for audits and inspections, promoting continuous improvement in statistical practices.
Top Skills: MS OfficePower BI
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Reposted 20 Days AgoSaved
Remote
US
136K-186K Annually
Mid level
136K-186K Annually
Mid level
Biotech
The Associate Director manages technology transfer for drug product development, collaborating with various stakeholders to ensure project success and maintaining manufacturing processes.
Top Skills: Analytical ChemistryChemical EngineeringPharmaceutical Science
Reposted 20 Days AgoSaved
Remote
US
27-27 Hourly
Internship
27-27 Hourly
Internship
Biotech
Support GxP Surveillance through monitoring regulatory requirements, daily screening of updates, and generating reports for regulators. No supervisory role involved.
Top Skills: ExcelMicrosoft 365MS OfficeMs TeamsOnedriveOutlookPowerPointSharepoint
21 Days AgoSaved
Remote
US
119K-159K Annually
Senior level
119K-159K Annually
Senior level
Biotech
The Contract Manager leads the administration and negotiation of clinical site contracts, ensuring compliance with regulations and timely delivery while overseeing a team to address issues and improve processes.
Top Skills: Contract Lifecycle Management SystemCtmsJIRAMS OfficeSharepointVeeva
Reposted 21 Days AgoSaved
Remote
US
206K-276K Annually
Senior level
206K-276K Annually
Senior level
Biotech
The Senior Director leads study start-up operations across North America, ensuring rapid site activation, managing budgets, and overseeing regulatory submissions while promoting continuous process improvements and team development.
Top Skills: Analytic ToolsMicrosoft Office SuiteTrial Management Applications
Reposted 21 Days AgoSaved
Remote
US
303K-383K Annually
Expert/Leader
303K-383K Annually
Expert/Leader
Biotech
Lead the Biologics IP team, oversee IP portfolio, provide legal counsel on patent and regulatory matters, and support R&D and commercialization efforts.
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