Clinical Research Coordinator

Job Description

We are seeking a skilled Clinical Research Coordinator to manage clinical trials from initiation to completion. This position will require strong organizational skills, attention to detail, and a passion for medical research.

Responsibilities

• Plan and coordinate clinical trial activities.
• Assist in preparing regulatory submissions and reports.
• Manage participant scheduling and follow-up appointments.
• Ensure data integrity and compliance with ethical standards.
• Act as a liaison between study sponsors and research sites.
• Organize and conduct study meetings and documentation reviews.

Requirements

Education

• Bachelor's degree in Life Sciences or a related field
• Postgraduate qualifications in Clinical Research is an advantage

Experience

• Minimum of 2 years experience in clinical research or trial management

Technical Skills

• Clinical Trial Management
• Data Analysis Software

Soft Skills

• Attention to Detail
• Communication

Certifications

• Clinical Research Coordinator Certification (CIRC)
• Good Clinical Practice (GCP) Certification

Languages

• English: Fluent

Advantageous

• Experience with electronic data capture (EDC) systems: Hands-on experience with EDC tools used for data collection in clinical trials.
• Familiarity with regulatory submission processes: Understanding of regulatory requirements and submission processes for clinical trials.

Benefits

• Competitive salary and benefits package
• Medical aid contribution
• Pension plan and retirement benefits
• Opportunities for professional development and training

Company Culture

• Collaborative Environment: We promote teamwork and collaboration across all levels of our organization.
• Innovation-Driven: With a focus on innovation, we strive to improve processes and outcomes in clinical research.
• Commitment to Diversity: We celebrate diversity and inclusiveness, ensuring a welcoming environment for everyone.