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Reposted YesterdaySaved
In-Office
Glendale, CA, USA
25-34 Hourly
Mid level
25-34 Hourly
Mid level
Pharmaceutical
The Clinical Enrollment Coordinator manages clinical trial enrollment, ensuring compliance with protocols, conducting screenings, and coordinating with teams to meet study requirements.
Top Skills: Clinical ResearchGood Clinical PracticesStandard Operating Procedures
Reposted 2 Days AgoSaved
In-Office
Glendale, CA, USA
25-34 Hourly
Junior
25-34 Hourly
Junior
Pharmaceutical
The Clinical Enrollment Coordinator will screen potential participants for clinical trials, manage enrollment processes, assist with documentation, and support compliance with clinical practices.
Top Skills: Clinical ResearchDatabase Management
Reposted 7 Hours AgoSaved
Remote
United States
Mid level
Mid level
Pharmaceutical
Lead strategic regulatory input for small molecule products, ensure compliance with global regulations, prepare documentation, and collaborate cross-functionally.
Top Skills: CredoEcatsTrackwise DigitalTrs Viewer
Reposted YesterdaySaved
Remote
United States
Senior level
Senior level
Pharmaceutical
The Senior Clinical Research Associate manages study sites, ensuring compliance with regulations and high performance. Responsibilities include site selection, monitoring, training site staff, and data management.
Top Skills: CtmsEtmf
Reposted YesterdaySaved
Remote
United States
Junior
Junior
Pharmaceutical
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.
Top Skills: Good Clinical Practices
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Reposted YesterdaySaved
Remote
United States
Senior level
Senior level
Pharmaceutical
Manage end-to-end labeling operations across global markets, ensure compliance with regulatory requirements, coordinate teams, and oversee drug safety activities.
Top Skills: Adobe AcrobatGlamsMS OfficePromomatsSharepointTrackwiseVeeva
Reposted YesterdaySaved
Remote
United States
Senior level
Senior level
Pharmaceutical
The Senior Regulatory Affairs Consultant will ensure compliance of promotional materials with US regulations, support product launches, and provide regulatory guidance across teams.
Top Skills: EdmsMS OfficeVeeva Promomats
Reposted YesterdaySaved
Remote
United States
Senior level
Senior level
Pharmaceutical
The Principal Biostatistician independently manages complex clinical trials, providing statistical support and leading studies with regulatory impact while contributing to business development and client interactions.
Top Skills: SAS
Reposted YesterdaySaved
Remote
United States
Mid level
Mid level
Pharmaceutical
As a Proposal Manager, you'll manage the proposal and contract processes, ensuring alignment with client specifications and collaborating across departments to deliver quality solutions on time.
Top Skills: DatabasesExcelOutlookSalesforceWindowsWord
Reposted YesterdaySaved
In-Office or Remote
3 Locations
Senior level
Senior level
Pharmaceutical
The General Manager oversees FSP programs, ensuring high-quality service delivery, financial management, account growth, and operational excellence, while maintaining customer relationships.
Top Skills: Financial Management SoftwareFsp EnvironmentProject Management Tools
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