Clinical Research Associate

Job Description

As a Clinical Research Associate, you will be instrumental in executing essential research protocols, monitoring patient care, and reporting clinical data. We are looking for a driven individual with a keen interest in medical research.

Responsibilities

• Conduct ongoing assessments of trial protocol adherence.
• Serve as a liaison between investigators and the sponsor company.
• Participate in the development of trial protocols, case report forms, and patient consent forms.
• Prepare for and assist with audits and inspections by regulatory authorities.
• Ensure the safety and welfare of trial participants.

Requirements

Education

• Bachelor's degree in Nursing, Pharmacy or related field
• Master's degree is a bonus

Experience

• 3+ years of experience in clinical trials or research

Technical Skills

• Clinical Trial Management
• Patient Management

Soft Skills

• Problem-solving
• Team Leadership

Certifications

• Clinical Research Coordinator (CRC) Certification

Languages

• English: Fluent

Advantageous

• Knowledge of statistical software (e.g., SAS, SPSS): Experience using statistical software for data analysis.
• Fluency in another local language: Ability to communicate in Afrikaans or Xhosa is advantageous.

Benefits

• Comprehensive medical aid covering family members
• Wellness programs and support
• Generous leave policies including annual and sick leave
• Employee assistance program

Company Culture

• Continuous Improvement: We foster a culture of excellence and ongoing personal and professional development.
• Accountability: Every team member takes ownership of their work and outcomes.
• Respect and Integrity: We uphold the highest standards of conduct in research and interactions.