Jobs at Novotech

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

The Project Oversight Director oversees multiple projects, manages client relationships, ensures resource allocation, monitors financial metrics, and leads a team of Senior Project Managers. They are responsible for driving client satisfaction and improving project delivery.

The Regulatory Start-Up Associate is responsible for the planning, preparation, and review of ethics and regulatory authority submissions for clinical trials, ensuring compliance with applicable guidelines and regulations.

The IT Analyst provides technical support within the IT service desk, resolves tickets, improves processes, and assists with IT projects.

The Regulatory Start Up Manager leads regulatory startup projects, collaborates with teams, oversees document submission, and manages compliance.

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

The Clinical Research Associate (CRA II/III) manages clinical trial activities, maintains communication with site personnel, ensures compliance with guidelines, and oversees participant recruitment and monitoring.

The Clinical Research Associate ensures trial participant rights and data integrity, manages site relationships, and oversees clinical trial compliance with regulations and guidelines.

The Senior HR Advisor provides people advisory support, manages employee relations, employee lifecycle processes, and ensures compliance with HR policies and legislation.

This entry-level role provides formal training and supervised experience in clinical trial conduct, site management, and regulatory compliance, supporting Clinical Research Associate activities.