Clinical Research Associate

Job Description

We are seeking a detail-oriented Clinical Research Associate to lead clinical trial initiatives in Pretoria. The ideal candidate will possess excellent organizational skills, a firm understanding of regulatory guidelines, and a strong ability to communicate effectively with stakeholders.

Responsibilities

• Oversee the collection and accuracy of clinical trial data.
• Serve as the primary point of contact for clinical trial sites.
• Implement and monitor compliance with GCP regulations and applicable local regulations.
• Contribute to the development of study protocols and updates.
• Assist with regulatory submissions and audits.

Requirements

Education

• Bachelor's degree in Health Sciences or related discipline
• Postgraduate qualifications in Clinical Research is beneficial

Experience

• 3+ years of clinical research experience preferred

Technical Skills

• Data Analysis
• Project Management

Soft Skills

• Adaptability
• Teamwork

Certifications

• Clinical Research Associate (CRA) certification
• Clinical Research Coordinator (CRC) certification

Languages

• English: Fluent

Advantageous

• Familiarity with electronic data capture systems: Understanding of systems used for capturing clinical trial data electronically.
• Knowledge of pharmacovigilance processes: Familiarity with monitoring drug safety and adverse events in clinical trials.

Benefits

• Comprehensive health insurance coverage
• Retirement savings plan
• Work from home options
• Ongoing training and development programs

Company Culture

• Continuous Improvement: We foster an environment where continuous learning and improvement are fundamental.
• Respect and Integrity: We value respect and integrity in our interactions with colleagues and participants alike.
• Innovative Thinking: We encourage innovative thinking and problem-solving at all levels of our organization.