Clinical Research Coordinator

Job Description

As a Clinical Research Coordinator based in Durban, you will play a vital role in the planning, implementation, and monitoring of clinical trials. You will work closely with investigators and study participants, ensuring compliance with regulatory requirements and maintaining high standards of patient safety.

Responsibilities

• Manage day-to-day clinical trial operations.
• Ensure adherence to study protocols and timelines.
• Perform data entry and maintain accurate study records.
• Participate in the development of study protocols.
• Liaise with healthcare professionals and patients for study needs.
• Monitor and report adverse events in a timely manner.

Requirements

Education

• Bachelor's degree in Nursing or related field
• Master's degree in Public Health is a plus

Experience

• 3+ years of experience in clinical trials or related areas

Technical Skills

• Project Management
• Regulatory Knowledge

Soft Skills

• Organizational Skills
• Team Leadership

Certifications

• Good Clinical Practice (GCP) Certification

Languages

• English: Fluent

Advantageous

• Experience with patient recruitment strategies: Skill in implementing effective strategies for recruiting study participants.
• Knowledge of GCP and ICH guidelines: Understanding of Good Clinical Practice and International Conference on Harmonisation guidelines.

Benefits

• Comprehensive medical and dental benefits
• Generous leave policies
• Career progression and training opportunities
• Work-life balance initiatives

Company Culture

• Diversity: We strive for a diverse workforce to bring varied perspectives to our research endeavors.
• Continuous Improvement: We foster a culture of continuous learning and professional growth for all team members.
• Community Engagement: We are actively involved in our community, promoting health and wellness through research.