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Biotech
Develops data-driven operational strategies for clinical trial proposals across non-oncology therapeutic areas. Reviews feasibility, budgets, timelines, recruitment plans, risks, and execution assumptions; creates proposal content and presents strategies during sponsor meetings and bid defenses. Partners with Business Development, Finance, Clinical Operations, Medical, and regional teams to align recommendations and transition awarded studies into execution. Supports process improvement, operational documentation, analytical tools, and cross-functional business acquisition activities.
Biotech
Lead end-to-end delivery of global clinical trials, managing project planning, budgets, cross-functional teams, vendor oversight, site activation, TMF/eTMF quality, regulatory compliance (ICH-GCP), risk mitigation, sponsor communications, and inspection readiness from start-up through close-out.
Biotech
Lead planning and execution of oncology clinical trials from site selection through close-out. Manage timelines, budgets, vendors, cross-functional teams, regulatory/GCP compliance, risk mitigation, and client communications to deliver projects on time and on budget.
