Top Tech Jobs & Startup Jobs in Los Angeles, CA

The Clinical Enrollment Coordinator manages the enrollment process for clinical trials, ensuring compliance with protocols and conducts screenings of potential participants. Responsibilities include quality control, data organization, and collaboration with team members to meet study requirements.

Conduct screening and protocol-specific participant visits, recruit and enroll study participants, maintain tracking systems and study logs, assist physicians with assessments, manage study supplies and samples, support monitoring visits, ensure participant safety and documentation accuracy, and comply with quality management and clinical operating guidelines.

Manage design, configuration, launch, monitoring, and close-out of electronic feasibility surveys. Ensure site/investigator readiness, maintain contact lists, track responses and CDAs, apply site identification strategy, and support risk mitigation for global feasibility assessments.

The Principal Biostatistician provides statistical support for clinical trials, leads analyses, and contributes to regulatory compliance and client meetings.

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.

The Clinical Scientist assists with clinical studies, supporting protocol leads, and liaising with stakeholders while ensuring compliance with standards.

Manage clinical laboratory studies, ensuring sample quality and data integrity by liaising with internal teams and external vendors, resolving issues related to clinical trials, and ensuring compliance with protocols.

Lead country/regional study operations from startup through close, overseeing CROs and site activation, managing timelines, budgets, risks, recruitment, vendor deliverables, and resolving escalations to ensure timely study delivery and compliance.

The Manager, Central Monitoring oversees centralized monitoring activities for clinical trials, analyzes data trends, and collaborates with study teams to ensure risk management and process improvements.

Lead lab operations by enhancing efficiency, managing projects, ensuring data integrity, and supporting clinical trials through effective programming and analysis.