Clinical Study Manager position focused on sponsor-dedicated clinical trial oversight across multiple European locations. The role involves designing and analyzing clinical trials, managing cross-functional teams, and ensuring regulatory compliance and data integrity throughout the study lifecycle.
Responsibilities
Oversee planning, execution, and monitoring of clinical trials for regulatory compliance and timelines
Collaborate with investigators, vendors, and internal stakeholders on successful study implementation
Develop and manage study budgets, resources, and timelines for efficient resource utilization
Lead resolution of issues and challenges during clinical trials using problem-solving and communication




Ensure data integrity and quality through rigorous monitoring and validation processes
Requirements
Bachelor's degree in scientific or healthcare-related discipline
Proven clinical study management experience with understanding of drug development and regulatory requirements
Strong project management skills with ability to handle multiple competing priorities
Excellent communication and interpersonal skills for cross-functional collaboration
Detail-oriented with focus on data accuracy and quality standards

📌 Clinical Study Manager (España)
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📍 España