Clinical Research Coordinator

Job Description

As a Clinical Research Coordinator, you will play a pivotal role in coordinating clinical trials from inception to conclusion. Your expertise will facilitate patient recruitment, data collection, and adherence to protocols in the Cape Town research setting.

Responsibilities

• Develop and implement study protocols in conjunction with research teams.
• Ensure participant safety and compliance with ethical standards.
• Facilitate communication between study sponsors, investigators, and regulatory bodies.
• Conduct ongoing training for staff on study procedures and compliance.
• Review and evaluate study reports and provide insights for improvements.

Requirements

Education

• Bachelor's degree in Life Sciences, Nursing, or related field
• Certification in Clinical Research (e.g., ACRP, SOCRA) is advantageous

Experience

• 2+ years of experience in clinical research or related roles

Technical Skills

• Clinical Trial Management
• Regulatory Knowledge

Soft Skills

• Attention to Detail
• Communication Skills

Certifications

• Certified Clinical Research Coordinator (CCRC)

Languages

• English: Fluent

Advantageous

• Experience with electronic data capture systems: Knowledge of EDC systems like REDCap or Medidata.
• Familiarity with GCP guidelines: Understanding of Good Clinical Practice and ethical standards.

Benefits

• Competitive salary and performance-based bonuses
• Comprehensive health insurance
• Opportunities for professional development
• Flexible working hours

Company Culture

• Innovation: We encourage innovative thinking and a collaborative environment.
• Integrity: Our team operates with transparency and ethical standards.
• Inclusivity: We celebrate diversity and foster an inclusive workplace.