Clinical Trials Coordinator

Job Description

As a Clinical Trials Coordinator, your main duties will involve planning, executing, and monitoring clinical trials to ensure adherence to regulatory guidelines and protocols while maintaining participant involvement and data integrity.

Responsibilities

• Implement strategies to enhance patient recruitment and retention.
• Document all trial-related activities and ensure compliance with regulatory requirements.
• Communicate with regulatory authorities and ethics committees as needed.
• Assist in analyzing trial data and preparing research findings for publication.
• Maintain up-to-date knowledge on industry trends and best practices related to clinical trials.

Requirements

Education

• Bachelor's degree in a related field.
• Master's degree or specialized training in clinical research is preferred.

Experience

• 3+ years in clinical trials or research coordination.

Technical Skills

• Clinical Trial Management
• Statistical Software

Soft Skills

• Team Leadership
• Problem Solving

Certifications

• Certified Clinical Research Associate (CCRA)
• Good Clinical Practice (GCP) Certification

Languages

• English: Fluent

Advantageous

• Advanced statistical analysis skills.: Ability to perform complex data analyses for trial reporting.
• Clinical data management experience.: Experience in managing clinical data to ensure quality and compliance.

Benefits

• Health care contributions and retirement benefits.
• Generous annual leave policy.
• Ongoing training and career progression opportunities.
• Supportive workplace culture.

Company Culture

• Excellence: We strive for excellence in all our trials, ensuring the highest standards of research integrity.
• Growth Opportunities: We provide ample opportunities for our team members to develop their skills and grow in their careers.
• Engagement: We value the contributions of all team members and encourage their active engagement in projects.