Senior Clinical Research Associate

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

📋 Description

• Overseeing clinical trial sites to ensure compliance with study protocols, regulatory standards, and Good Clinical Practice (GCP) guidelines.

• Performing site visits to evaluate site performance, address challenges, and offer support for successful trial implementation.

• Working collaboratively with cross-functional teams to ensure prompt and precise data collection and reporting.

• Delivering training and support to site personnel and other Clinical Research Associates (CRAs) to uphold high standards of clinical trial management.

• Establishing and nurturing productive relationships with site staff and stakeholders to ensure efficient trial operations.

⛳️ Requirements

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

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

• Demonstrated capability to oversee multiple sites and projects concurrently, exhibiting strong organizational and problem-solving abilities.

• Proficiency in monitoring practices, maintaining data integrity, and managing sites, along with expertise in relevant clinical trial software and tools.

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

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

🏝️ Benefits

• Competitive base salary along with performance-related incentives.

• Health and wellness programs, including medical, dental, and vision coverage where applicable.

• Retirement and pension plans.

• Life insurance and disability coverage.

• Employee assistance programs and wellness resources.

• Opportunities for learning and development through structured training and career advancement pathways.