Clinical Research Coordinator

Job Description

As a Clinical Research Coordinator, you will play a pivotal role in managing clinical trials from inception to completion. Your insights and expertise will ensure compliance with all regulatory standards while facilitating seamless collaboration between research teams and clinical sites.

Responsibilities

• Oversee the execution of clinical trials, ensuring adherence to protocol.
• Serve as the primary contact for regulatory bodies and study sponsors.
• Ensure that all documentation is accurately completed and stored.
• Organise and lead meetings to discuss trial progress.
• Work closely with data management teams to ensure timely data entry.
• Training new staff members on procedures and compliance requirements.
• Conduct site visits to ensure compliance and support.
• Prepare budgets and monitor expenses throughout the project lifecycle.

Requirements

Education

• Master's degree in a relevant field preferred

Experience

• 5+ years of experience in clinical trials management

Technical Skills

• EDC Systems
• Statistical Analysis Software

Soft Skills

• Attention to detail
• Time management

Certifications

• Clinical Research Associate (CRA)
• ISO 9001 Certification

Languages

• English: Fluent

Advantageous

• Certification in project management: Desirable to have a recognised project management certificate.
• Experience with virtual study management: Experience in managing remote study teams effectively.

Benefits

• Comprehensive health benefits.
• Flexible work options and remote working.
• Paid training and development programs.
• Wellness initiatives and support.

Company Culture

• Professional Growth: We prioritize the professional development of our staff. Continuous learning is vital to our success.
• Inclusivity: Diversity and inclusion are at the core of our culture, providing a welcoming space for all.
• Community Engagement: We strive to give back to the community and engage in initiatives that promote health and wellbeing.