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Biotech
Manage site relationships and monitor clinical trial conduct to ensure participant safety and data integrity. Perform site initiation, monitoring, and close-out visits (on-site or remote), maintain TMF and CTMS, support regulatory/ethics submissions, drive site recruitment, report study progress, and ensure audit/inspection readiness per ICH GCP and Sponsor/Novotech SOPs.
Biotech
Lead clinical systems and technology initiatives across the study lifecycle: govern and deliver clinical platforms (Veeva, Obvio), define standardised reporting and KPIs (Power BI, Excel), identify and prioritise clinical AI/automation use cases, translate business needs into IT-compliant solutions, drive adoption/compliance, and manage cross-functional projects with QA, IT, Biometrics, PM, Medical, and Operations stakeholders.
Biotech
The Contracts Manager ensures accurate and compliant contract processing, collaborates with Sales and Legal, identifies risks, and drives operational excellence.
