Clinical Research Coordinator

Job Description

Join our team as a Clinical Research Coordinator where you will play a critical role in directing and executing medical research projects, guaranteeing that all work aligns with ethical standards while fostering a collaborative research environment.

Responsibilities

• Lead recruitment strategy for clinical trials, focusing on diversity and inclusion.
• Ensure compliance with institutional review board (IRB) requirements.
• Act as the primary point of contact for trial participants.
• Implement and monitor quality assurance measures.
• Prepare and present findings of research projects.
• Maintain relationships with external regulatory bodies.
• Collaborate with various departments to align research objectives.
• Conduct training workshops for staff on current clinical research standards.
• Assist in developing standard operating procedures (SOPs).
• Provide logistical support during clinical trial execution.

Requirements

Education

• Bachelor's degree in Health Sciences or related field
• Master's is preferred

Experience

• 3+ years of experience in clinical trials

Technical Skills

• Patient recruitment
• Statistical software proficiency

Soft Skills

• Team leadership
• Problem-solving

Certifications

• Good Clinical Practice (GCP) Certification

Languages

• English: Fluent
• Zulu: Basic

Advantageous

• Experience in conducting site audits: Experience with conducting clinical trial site audits for compliance.
• Knowledge of patient safety regulations: Solid understanding of patient safety protocols in clinical research.

Benefits

• Comprehensive health insurance and wellness programs
• Paid time off and flexible work hours
• Career growth opportunities through advanced training
• Engaging company culture that prioritizes teamwork

Company Culture

• Innovation: We encourage innovative thinking and welcome new ideas.
• Community Focus: We are committed to giving back to the community through outreach.