Clinical Research Associate

Job Description

As a Clinical Research Associate based in Johannesburg, you will oversee all aspects of clinical trials, including monitoring patient safety, data management, and liaising with stakeholders to meet compliance demands.

Responsibilities

• Monitor site performance and take corrective actions when necessary.
• Collaborate with multidisciplinary teams to streamline study processes.
• Act as the primary contact for study-related queries.
• Generate reports on study progress and outcomes for internal and external stakeholders.
• Facilitate communication between stakeholders, including sponsors and regulatory bodies.

Requirements

Education

• Bachelor's degree in a health-related field
• Master's degree in Clinical Research is preferred

Experience

• 3+ years of experience in clinical trials or monitoring

Technical Skills

• Regulatory Compliance
• Project Management

Soft Skills

• Problem-solving Skills
• Interpersonal Skills

Certifications

• Certified Clinical Research Associate (CCRA)
• Clinical Research Coordinator (CRC) Certification

Languages

• English: Fluent

Advantageous

• Knowledge of Good Clinical Practice (GCP): Solid grounding in GCP standards and implementation.
• Experience in data analysis and report generation: Proficient in generating reports based on clinical trial data.

Benefits

• Attractive compensation structure
• Comprehensive health and wellness benefits
• Educational reimbursement programs
• Paid time off and sick leave
• Employee assistance programs

Company Culture

• Growth and Development: We invest in our employees' professional growth through training and support.
• Diversity and Inclusion: We value diverse perspectives and backgrounds within our teams.
• Work-Life Balance: We strive to create a work environment that supports both personal and professional commitments.