Clinical Research Coordinator

Job Description

As a Clinical Research Coordinator, you will oversee clinical trials from inception to completion. Responsibilities include monitoring participant safety, managing timelines, and maintaining study documentation. This is a fantastic opportunity to contribute to cutting-edge medical research.

Responsibilities

• Assist in the development of study protocols and materials.
• Monitor participant progress and safety throughout the study.
• Prepare reports for regulatory submissions and audits.
• Conduct site visits and monitor compliance with study protocols.
• Provide training and support to site personnel involved in the study.

Requirements

Education

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

Experience

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

Technical Skills

• Clinical Research
• Data Management

Soft Skills

• Attention to Detail
• Interpersonal Skills

Certifications

• Certified Clinical Research Coordinator (CCRC)
• Good Clinical Practice (GCP) Certification

Languages

• English: Fluent

Advantageous

• Experience with statistical software: Familiarity with software such as SPSS or SAS for data analysis.
• Knowledge of regulatory requirements: Understanding of SA regulatory standards for clinical trials.

Benefits

• Medical aid and wellness benefits
• Paid leave and public holidays
• Professional development opportunities
• Flexible working arrangements

Company Culture

• Collaboration: Our team values collaboration and open communication, fostering a supportive work environment.
• Innovation: We encourage innovative thinking and new ideas to enhance our research outcomes.
• Commitment to Excellence: We strive for excellence in our research to improve healthcare and patient outcomes.