This is a fully remote position, open to applicants in Spain.

📋 Description

• Supervise and coordinate clinical trial activities in accordance with the protocol, regulatory guidelines, and industry standards.

• Lead monitoring tasks for clinical trials that require technical expertise, emphasizing quality and ongoing improvement.

• Ensure clinical trial sites comply with study protocols, regulatory standards, and Good Clinical Practice (GCP) guidelines.

• Perform site visits to evaluate performance, address challenges, and facilitate effective trial execution.

• Work collaboratively with cross-functional teams to ensure timely and accurate data collection and reporting.

• Offer training and support to site personnel and other Clinical Research Associates (CRAs).

• Establish and nurture relationships with site staff and stakeholders.

⛳️ Requirements

• Bachelor's degree in a relevant scientific field or healthcare-related discipline.

• Significant experience as a Clinical Research Associate, with a comprehensive understanding of clinical trial processes and regulatory requirements.

• Demonstrated ability to manage multiple sites and projects concurrently, possessing strong organizational and problem-solving capabilities.

• Proficiency in monitoring practices, data integrity, and site management, along with familiarity with pertinent clinical trial software and tools.

• Exceptional communication, interpersonal, and stakeholder management skills, with the capacity to influence and ensure compliance in a complex environment.

• Willingness to travel as needed (approximately 60%).

• Legal authorization to work in Spain.