Clinical Research Associate

Job Description

Join our dynamic team as a Clinical Research Associate in Cape Town. This role involves managing clinical trials from initiation to completion, ensuring regulatory compliance, and liaising with participants and healthcare providers to gather essential data.

Responsibilities

• Coordinate and manage all aspects of clinical trials from start to finish.
• Monitor and track budgets, timelines, and project milestones.
• Liaise with institutional review boards (IRBs) for approvals and compliance.
• Facilitate data entry and data management processes.
• Implement corrective actions when deviations from the protocol are identified.
• Ensure timely completion of study milestones and adherence to timelines.
• Support the clinical research team with administrative tasks as needed.

Requirements

Education

• Bachelor's in Nursing, Life Sciences or relevant field
• Master's in Clinical Research preferred

Experience

• 5+ years of clinical research experience

Technical Skills

• Project Management
• Clinical Monitoring

Soft Skills

• Interpersonal Skills
• Critical Thinking

Certifications

• Certified Clinical Research Associate (CCRA)
• Clinical Research Associate Qualification (CRQ)

Languages

• English: Fluent

Advantageous

• Familiarity with Electronic Health Records (EHR): Understanding of EHR systems utilized in clinical settings.
• Experience in Multi-Site Trials: Knowledge of managing trials across several healthcare sites.

Benefits

• Medical aid and dental cover
• Retirement savings plan with company contribution
• Generous annual leave and public holidays
• Professional development opportunities

Company Culture

• Community Impact: Our work positively impacts the community, improving health outcomes through research.
• Continuous Growth: We provide ample opportunities for professional growth and personal development.
• Work-Life Balance: We promote work-life balance, ensuring our employees feel supported in all aspects of their lives.