Jobs at Novotech

The Project Specialist assists the Project Manager in managing project deliverables, finances, timelines, and liaising with clinical teams for project success.

The Project Manager oversees clinical projects from site selection to closeout, ensures compliance with regulations, manages risks, and maintains client relationships.

The Senior Director of Quality Assurance leads the global Quality Management System, ensuring regulatory compliance, operational excellence, and quality strategy aligned with organizational goals. They oversee audits, support client engagements, and manage a high-performing QA team through budget and resource allocation.

The Clinical Research Associate manages relationships with site personnel to ensure clinical trials comply with regulatory standards and protect participant wellbeing, while overseeing site monitoring and data accuracy.

The Proposals Manager leads the proposal lifecycle, collaborates with teams to develop strategies, creates pricing models, and manages internal reviews for submissions.

The Director Centralized Clinical Monitoring oversees Risk-Based Quality Management and centralized monitoring strategies, ensuring high-quality clinical trials and leading multidisciplinary teams.

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 Inhouse Clinical Research Associate supports clinical team activities, manages study documentation, and ensures compliance with regulatory standards.

The Clinical Research Associate (CRA) manages site relationships, ensures trial compliance, supports recruitment, and verifies trial data. They maintain documentation and facilitate regulatory submissions while monitoring site performance.

The Contracts Manager ensures accurate and compliant contract processing, collaborates with Sales and Legal, identifies risks, and drives operational excellence.

The Regulatory Start-Up Associate manages submissions for clinical trials, ensuring compliance with regulations and timelines while coordinating cross-functional efforts and stakeholder communication.