Clinical Research Coordinator

Job Description

We are looking for a proactive Clinical Research Coordinator who will lead our clinical trials in Durban. This role involves managing project logistics, maintaining compliance, and liaising with clinical staff and participants.

Responsibilities

• Manage the coordination and implementation of clinical research projects.
• Oversee data collection, reporting, and analysis to ensure compliance with protocol requirements.
• Collaborate with medical and scientific professionals to enhance trial recruitment.
• Prepare and submit regulatory documents to ethics committees and regulatory agencies.
• Maintain a thorough understanding of the research protocol and GCP guidelines.
• Provide support for study meetings, including participant training sessions.
• Facilitate communication between various stakeholders to ensure project success.
• Monitor the safety and well-being of trial participants.

Requirements

Education

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

Experience

• Minimum 3 years of experience in clinical research

Technical Skills

• Clinical Trial Management
• Data Analysis

Soft Skills

• Communication
• Organizational Skills

Certifications

• Certified Clinical Research Coordinator (CCRC)
• GCP Certification

Languages

• English: Fluent

Advantageous

• Experience with patient recruitment strategies: Experience in developing effective strategies to recruit participants for clinical trials.
• Knowledge of regulatory submissions: Understanding of the process for submitting clinical trial applications.

Benefits

• Health and wellness benefits
• Professional development opportunities
• Flexible work hours
• Team-building events

Company Culture

• Teamwork: We value collaboration and teamwork to achieve our research goals.
• Innovation: We encourage innovative thinking and approaches in our research projects.
• Integrity: Our commitment to integrity ensures that we conduct our research responsibly and ethically.