Travel Clinical Research Associate - Remote

Overview

The Travel Clinical Research Associate (CRA) plays a vital role in the Alira Health Clinical team, conducting site monitoring for clinical trials while ensuring compliance and quality through collaboration with various stakeholders.

In Short

• Conduct site monitoring for clinical trials.
• Ensure compliance with protocols and regulations.
• Provide oversight and guidance to the CRA team.
• Manage study budgets and billing information.
• Perform qualification, initiation, interim, and close-out visits.
• Maintain regular contact with study sites.
• Participate in training and mentoring of new CRAs.
• Collaborate on Clinical Trial Management System (CTMS).
• Travel 60-80% for site visits.
• Develop problem-solving strategies for site issues.

Requirements

• Bachelor's degree in a scientific health field.
• Certification as a Monitor in compliance with local regulations.
• Strong organizational and analytical skills.
• Ability to manage multiple priorities in a fast-paced environment.
• Excellent communication and interpersonal skills.
• Knowledge of clinical research and ethical requirements.
• Proficient in using clinical trial management systems.
• Ability to travel frequently.
• Professional and disciplined work ethic.
• Strong command of local language and English.

Benefits

• Professional development opportunities.
• Global travel experiences.
• Flexible work programs.
• Collaborative work environment.
• Supportive team culture.
• Access to a diverse range of expertise.
• Innovative technologies in healthcare.
• Comprehensive benefits package.
• Opportunities for advancement.
• Involvement in impactful projects.