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)
🏢 Icon
📍 España