Clinical Research Associate

Job Description

Join our team as a Clinical Research Associate in Cape Town, where you will oversee clinical trial operations, manage relationships with study sites, and ensure regulatory compliance throughout the trial process.

Responsibilities

• Lead site monitoring visits and provide support to study sites throughout the trial process.
• Collaborate with data management teams to ensure data integrity and compliance.
• Report adverse events and serious adverse events in accordance with regulatory guidelines.
• Participate in the development and review of study-related documents.
• Manage relationships with external vendors involved in the clinical trials.
• Implement corrective actions as needed to resolve compliance issues.

Requirements

Education

• Bachelor's degree in Health Sciences or related discipline
• Certification in Clinical Research is preferred

Experience

• 2-4 years of clinical research experience

Technical Skills

• Protocol Development
• Regulatory Compliance

Soft Skills

• Interpersonal Skills
• Problem-Solving

Certifications

• Clinical Research Coordinator Certification (CRCC)
• Certified Clinical Research Associate (CCRA)

Languages

• English: Fluent

Advantageous

• Understanding of statistical analysis: Knowledge of statistical methods and their application in clinical research.
• Familiarity with international regulatory guidelines: Experience with global regulations impacting clinical trials.