Teams at Novotech

Lead clinical trial projects from site selection through study close-out, serving as primary client contact. Oversee cross-functional teams, vendors, budgets, timelines, risk management, site training, recruitment, safety reporting, eTMF/CTMS maintenance, and audit/inspection readiness while ensuring compliance with ICH GCP, local regulations, SOPs and Project Agreement.

Reviews, amends, negotiates, and executes Clinical Trial Agreements with research sites. The role ensures contracts comply with legal requirements, internal policies, and negotiation parameters while supporting timely clinical trial start-up and maintenance. Responsibilities include managing contract workloads, assessing risks, escalating issues, coordinating with Project Management, Regulatory, Clinical Operations, Finance, Legal, study teams, clients, and sites, and facilitating company signatory execution.

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.