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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 Senior Clinical Research Associate manages site monitoring and relationships for clinical trials, ensuring compliance and patient safety according to GCP and regulations.

This role involves leading lab operations, streamlining processes, and supporting sample data integrity for clinical trials while managing teams and vendor relationships.

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

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 design and reporting of end-to-end labeling KPIs and dashboards, ensure data integrity and governance, support compliance forums, audits, and digital enablement, and provide analytic insights to drive process improvements and CAPAs while offering cross-trained operational backup.

Lead end-to-end labeling process management including deviation/CAPA investigations, process governance, systems stewardship (Veeva RIMS, TrackWise, QDocs, Documentum), audit and inspection readiness, and cross-functional process improvements. Develop training and support regulatory intelligence, ensuring compliant labeling operations, KPI oversight, and coordination with Regulatory, Pharmacovigilance, Quality, and Manufacturing.

The Sr. Clinical Research Associate manages clinical trial sites, ensuring compliance with regulations, monitoring study conduct, and supporting investigators. Key duties include site selection, training, risk management, and data quality assurance.

The role involves leading regulatory CMC strategy for peptide and oligonucleotide therapeutics, driving submissions, and ensuring compliance with relevant standards.