Clinical Trials Coordinator

Job Description

As a Clinical Trials Coordinator, you will play a key role in the management and execution of clinical trials, ensuring compliance with regulatory standards and protocols. You will liaise with investigators, monitor trial progress, and manage data collection to support our research goals and improve healthcare outcomes.

Responsibilities

• Lead projects from conception to completion, ensuring trials are conducted on time and within budget.
• Engage with stakeholders to report on trial progress and outcomes.
• Implement quality assurance processes to improve operational efficiency.
• Prepare progress reports for management and funding bodies.
• Assist in the development of promotional materials for clinical trials.
• Support data management teams with data entry and management.
• Coordinate with clinical staff for training and protocol adherence.

Requirements

Education

• Bachelor's degree in Nursing or related field
• Clinical Research Certification is a plus

Experience

• 3-5 years of experience in clinical research or healthcare settings

Technical Skills

• Clinical Monitoring
• Statistical Software

Soft Skills

• Problem-solving
• Leadership

Languages

• English: Fluent

Advantageous

• Experience in Patient Recruitment: Proven ability to recruit and retain trial participants effectively.
• Training in Clinical Trial Management: Certification or training courses in clinical trial management would be beneficial.

Benefits

• Comprehensive medical aid and retirement plans
• Professional development programs
• Supportive work environment
• Paid time off and holidays

Company Culture

• Diversity and Inclusion: We value diversity and strive to create an inclusive environment for all employees.
• Professional Growth: We provide our employees with opportunities for continuous learning and career advancement.