Senior Trial Manager (Sponsor Dedicated, Multiple Therapeutics)

The role involves overseeing sponsor-dedicated clinical studies across multiple sites, with responsibilities including site selection, recruitment strategy, regulatory compliance, vendor management, and serving as the primary sponsor contact at the country level. Key duties include Leading site qualification activities and feasibility assessmentsDeveloping and executing country-specific recruitment plans to ensure enrollment and data qualityMaintaining trial management systems, monitoring study progress, and implementing corrective actionsManaging budgets, vendor performance, invoices, and financial forecasts Qualifications And Skills Advanced knowledge of GCP and regulatory standardsExperience managing complex clinical trial setups at the country levelProficiency with trial management tools such as CTMS, eTMF/IFExpertise in site selection, qualification, and performance optimizationStrong financial management, budget forecasting, and vendor oversight skillsAbility to develop contingency plans and identify risks at the country level