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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.

Lead global study start-up and site activation for Phase I-III and real-world trials. Develop global start-up plans, partner with CROs and stakeholders, forecast enrollment, track KPIs, remove activation barriers, and mentor junior staff to ensure timely, high-quality study delivery.

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 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.

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.