Clinical Research Coordinator

Job Description

We are seeking a Clinical Research Coordinator to oversee clinical trials and ensure compliance with regulatory requirements. The ideal candidate will have a solid understanding of clinical trial processes and excellent organizational skills.

Responsibilities

• Monitor compliance with regulatory standards throughout clinical trials.
• Guide recruitment processes for clinical trials, ensuring diverse participant selection.
• Prepare detailed reports on trial findings for internal and external stakeholders.
• Collaborate effectively with multidisciplinary teams, including data managers and medical writers.
• Assist in the development of training materials for trial staff.
• Conduct presentations on trial protocols and progress to management and stakeholders.

Requirements

Education

• Bachelor's degree in nursing or pharmacy
• Master's degree in clinical research preferred

Experience

• 5+ years managing multicentre clinical trials

Technical Skills

• EDC Systems
• Clinical Trial Management Systems (CTMS)
• Statistical Analysis Software (SAS or R)

Soft Skills

• Leadership
• Attention to Detail

Certifications

• Clinical Research Associate (CRA)
• GCP Certification

Languages

• English: Fluent
• Xhosa: Conversational

Advantageous

• Managing Adaptive Design Trials: Hands-on experience managing adaptive design trials.
• Experience with Diverse Populations: Experience working with diverse study populations is beneficial.

Benefits

• Comprehensive health cover with additional wellness programs.
• Pension fund contributions.
• Employee wellness initiatives.
• Opportunity to work in a collaborative team environment.

Company Culture

• Continuous Improvement: We encourage ongoing learning and skill development among our staff.
• Diversity: Our culture embraces diversity in all forms, enhancing our work environment.
• Innovation: Innovation is at the heart of our operations and clinical research.