Clinical Research Associate

Job Description

We are seeking a Clinical Research Associate to join our dynamic team in Cape Town. The ideal candidate will be responsible for coordinating and managing clinical trials, ensuring compliance with regulatory standards, and contributing to the advancement of medical research.

Responsibilities

• Oversee the full lifecycle of clinical trials, ensuring adherence to timelines.
• Conduct site initiation visits and training for site staff.
• Review and validate trial-related documentation.
• Work with the data management team to ensure data integrity.
• Assist in the preparation of regulatory submissions.
• Engage in problem-solving and provide solutions to trial challenges.
• Document all trial-related activities and maintain a comprehensive study file.

Requirements

Education

• Bachelor's degree in Nursing or related health field
• Master's degree in Clinical Research or related field is preferred

Experience

• 4+ years of experience in clinical trials and research

Technical Skills

• Project Management
• Protocol Development

Soft Skills

• Interpersonal Skills
• Organizational Skills

Certifications

• Advanced Clinical Research Coordinator (ACRC)

Languages

• English: Fluent

Advantageous

• Familiarity with data management software: Experience with software tools for data management in clinical settings.
• Experience with patient recruitment strategies: Understanding of patient recruitment and retention techniques.

Benefits

• Comprehensive health insurance
• Generous leave policies
• Favorable retirement plans
• Continuous learning and development

Company Culture

• Patient-Centric Approach: Our focus is always on improving patient outcomes, making our work meaningful.
• Continuous Improvement: We encourage ongoing learning and improvements in our processes.