Clinical Research Associate

Job Description

Join our esteemed team as a Clinical Research Associate, where you'll play a vital role in the implementation of clinical studies. You will ensure adherence to protocols and contribute to the advancement of medical research.

Responsibilities

• Assist in the development of trial protocols and informed consent templates.
• Lead site training sessions and provide ongoing support to site staff.
• Evaluate site compliance through regular monitoring visits.
• Prepare for audits by regulatory agencies and sponsors.
• Act as a liaison between sponsors and institutions.

Requirements

Education

• Bachelor's degree in Nursing or a related field
• Advanced degree in a relevant discipline is preferred

Experience

• 5+ years of experience in clinical trial coordination

Technical Skills

• Data Analysis
• Project Management

Soft Skills

• Critical Thinking
• Team Leadership

Certifications

• International Conference on Harmonisation (ICH) Training Certificate

Languages

• English: Fluent
• Zulu: Basic

Advantageous

• Skill in statistical analysis software: Experience using software packages like SPSS or SAS for data analysis.
• Certification in Good Clinical Practice (GCP): Holder of certification in GCP standards.

Benefits

• Comprehensive health insurance with dental and vision cover.
• Subsidized gym membership and wellness programs.
• Paid parental leave and vacation days.
• Reimbursement for professional memberships.

Company Culture

• Continuous Improvement: We encourage continuous improvement and learning for all employees.
• Inclusion and Diversity: Our workplace is inclusive and welcomes diverse perspectives.
• Community Engagement: We engage with the community to promote health and wellness initiatives.