Clinical Research Associate

Job Description

We are looking for a Clinical Research Associate to join our dedicated team in Pietermaritzburg. The ideal candidate will oversee clinical trials, ensuring compliance with regulatory guidelines, and collaborating with healthcare professionals to collect and analyze data effectively. Your role will also involve preparing detailed reports and contributing to the development of new treatment protocols.

Responsibilities

• Oversee regulatory compliance during all trial stages.
• Organize and prepare for site initiation and close-out visits.
• Develop and maintain relationships with participating sites and stakeholders.
• Review and evaluate trial protocols to ensure feasibility and compliance.
• Conduct site audits and ensure standard operating procedures are followed.

Requirements

Education

• Bachelor's degree in a relevant field
• Master's degree in Clinical Research or related field is preferred

Experience

• 3+ years of experience in clinical trials or research setting

Technical Skills

• Clinical Research Methodology
• Statistical Analysis

Soft Skills

• Problem-solving
• Organization

Certifications

• Clinical Research Coordinator Certification
• Clinical Trials Management Certification

Languages

• English: Fluent

Advantageous

• Experience with electronic data capture systems: Proficient in using EDC systems for data collection.
• Familiarity with international clinical trial guidelines: Understanding of ICH/GCP guidelines and their application.

Benefits

• Comprehensive health and dental insurance
• Annual performance bonuses
• Flexible benefits package
• Access to training and career advancement programs

Company Culture

• Growth: We provide numerous opportunities for personal and professional growth in a supportive environment.
• Inclusivity: Diversity is at the heart of our institute, and we strive for inclusivity in every project and team.
• Accountability: We believe in accountability for actions, promoting a culture of responsibility and trust.