Novartis
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Biotech • Pharmaceutical
Oversee quality, completeness, and readiness of Trial Master Files across a global portfolio. Identify documentation risks and trends, lead vendor oversight, drive remediation and continuous improvement, support audit readiness, and act as TMF subject-matter expert while supporting resource planning and innovation initiatives.
Biotech • Pharmaceutical
Lead identification, evaluation, and implementation of operational innovations (especially AI-driven) across clinical trial portfolios. Influence stakeholders, assess value/risk, integrate solutions into execution plans, support trial teams, and scale successful technologies to improve recruitment, access, and trial efficiency.
Biotech • Pharmaceutical
The role involves leading clinical data management tasks, ensuring quality and compliance in data for clinical trials, collaborating with teams, and supporting junior staff.
