Top Tech Jobs & Startup Jobs in Belfast

Manage clinical trial supplies, ensure compliance with GMP and GCP, oversee vendor management, and maintain project information for studies.

Ensure effective clinical research operations, monitor study progress, adhere to regulations, and coordinate communication with clinical trial participants.

The On-site Monitor will manage site activities, ensure compliance with regulations and guidelines, support data collection, and maintain communication with site staff and the project team.

The Principal R/RShiny Programmer will develop statistical programming standards, provide technical leadership, mentor junior programmers, and ensure data integrity.

Manage interdisciplinary clinical research projects, ensuring compliance and timely execution while maintaining quality and financial performance. Act as liaison with clients and manage project teams.

Responsible for managing team performance, customer delivery, and business impact while leading FSP360 multifunctional staff. Ensures alignment with KPIs, fosters customer relationships, handles resource management, and supports team members' development.

The Senior Proposal Analyst prepares and manages proposal documents and budgets, collaborates with team members, and ensures alignment with RFP requirements.

The CRA II conducts site monitoring, ensures regulatory compliance, manages site activities, and supports project objectives while assessing site performance and patient safety.

The role involves developing and maintaining R-based applications, mentoring biostatisticians, overseeing projects, and ensuring statistical quality and compliance in clinical trials.

The role involves site management activities including monitoring, compliance checks, report documentation, and maintaining relationships with study site personnel. It requires familiarity with GCP and regulatory guidelines, along with managing site-specific actions and communication.