Clinical Research Coordinator

Job Description

Seeking a detail-oriented Clinical Research Coordinator to lead clinical study activities in Pretoria. Responsibilities include managing patient outreach, maintaining study databases, and coordinating with researchers and participants to ensure timely trial execution.

Responsibilities

• Oversee patient recruitment processes and maintain communication with participants regarding study progress.
• Review and monitor study inventory and supplies to ensure proper stock levels.
• Prepare regular updates and reports for management regarding trial progress and challenges.
• Ensure all clinical trial protocols are followed precisely for data integrity and compliance.
• Conduct site visits to monitor the quality and integrity of the trial processes.
• Implement corrective actions as needed to resolve any compliance issues.

Requirements

Education

• Master's degree in Clinical Research or related field

Experience

• 5+ years of experience in clinical trial management

Technical Skills

• Regulatory Compliance
• Project Management Software

Soft Skills

• Leadership
• Adaptability

Certifications

• Good Clinical Practice (GCP) Certification
• Clinical Research Associate Certification

Languages

• English: Fluent

Advantageous

• Experience with Electronic Data Capture (EDC): Knowledge of systems used for capturing clinical data electronically.
• Familiarity with Statistical Software Packages: Ability to analyze data using statistical software like SPSS or SAS.

Benefits

• Full medical cover for employees and their families
• Employee assistance programs
• Continuous learning and development opportunities
• Work-life balance initiatives

Company Culture

• Continuous Improvement: We are dedicated to continuous improvement in all aspects of our work and employee development.
• Respect for Individuals: Each team member is respected, and their ideas are valued and considered.
• Health and Well-being: We prioritize the health and well-being of our employees in the workplace.