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The Clinical Research Associate is responsible for managing relationships with trial sites, ensuring data integrity, compliance with regulations, and supporting trial participant recruitment.

The Senior Clinical Research Associate ensures participant welfare and accuracy of trial data, managing site operations and relationships, overseeing compliance with guidelines, and supporting trials in both remote and on-site capacities.

The Principal Clinical Data Programmer leads clinical data programming for multiple studies, ensuring adherence to quality standards and SOPs while developing and maintaining clinical trial databases using EDC applications and integrating study data.

The Project Manager - Early Phase leads early phase clinical research projects, ensuring feasibility, project management, vendor coordination, and compliance with project standards while managing timelines and team collaboration.

The Project Specialist supports project management by assisting with deliverables, cost control, and maintaining project plans and tracking systems, specifically in clinical research.

The Director leads drug development consulting engagements, focusing on clinical pharmacology strategies, regulatory submissions, mentoring juniors, and business development in a collaborative life-sciences context.

The Clinical Research Associate manages trial participant relations and ensures accuracy in trial data through adherence to GCP guidelines and regulations.

The Regulatory Start Up Associate II manages ethics and regulatory applications during clinical trial start-up, ensuring compliance with local regulations.