Clinical Research Associate

Job Description

As a Clinical Research Associate at our Pretoria facility, you will play a crucial role in the management and monitoring of clinical trials, ensuring compliance with regulatory requirements. You will collaborate closely with cross-functional teams and contribute to impactful research that advances healthcare solutions.

Responsibilities

• Implement clinical trial protocols and conduct feasibility assessments.
• Coordinate recruitment strategies for study participants.
• Review and approve informed consent documents.
• Provide updates and communicate findings to stakeholders.
• Assist in regulatory submissions and compliance checks.
• Evaluate site performance and assist in site selection.

Requirements

Education

• Bachelor's degree in Biomedical Science or related field
• Master's degree is advantageous

Experience

• 3-5 years of clinical trial experience preferred

Technical Skills

• Data Management
• Patient Interaction

Soft Skills

• Critical Thinking
• Teamwork

Certifications

• Registered Nurse (RN)
• Clinical Research Associate (CRA)

Languages

• English: Fluent

Advantageous

• Experience in pharmacovigilance: Knowledge in monitoring and assessing adverse drug reactions.
• Published research experience: Having published research articles in reputable journals is a plus.

Benefits

• Comprehensive health benefits for employees and families
• Annual leave and personal days
• Professional development support
• Employee recognition programs

Company Culture

• Respectful Collaboration: We encourage respectful collaboration among team members, with a focus on mutual support and growth.
• Continuous Learning: We support ongoing education and training opportunities to enhance our team's skills and knowledge.
• Community Impact: Our research initiatives aim to improve community health outcomes, and our team is passionate about making a difference.