Clinical Research Coordinator

Job Description

We are seeking a Clinical Research Coordinator responsible for overseeing clinical trials to ensure compliance with protocols and regulatory requirements. This role includes conducting site visits, reviewing documentation, and supporting study personnel.

Responsibilities

• Ensure compliance with Good Clinical Practice (GCP)
• Evaluate regulatory submissions and documentation
• Facilitate communication between clinical sites and sponsors
• Conduct training sessions for site staff on trial protocols
• Interpret regulatory guidelines to ensure compliance
• Manage and track study supplies and documentation
• Document and report adverse events as per regulatory standards
• Produce statistical reports on trial progress

Requirements

Education

• Bachelor's degree in a healthcare-related field

Experience

• Experience in managing clinical trials is an advantage

Technical Skills

• EDC Systems
• Database Management

Soft Skills

• Problem-solving
• Team Collaboration

Languages

• English: Fluent

Advantageous

• Regional language proficiency: Ability to communicate in a regional language can be advantageous.
• Experience with electronic informed consent (eConsent) processes: Hands-on experience with eConsent systems is a plus.

Benefits

• Comprehensive health coverage and wellness benefits
• Generous leave policies including annual and sick leave
• Professional development and training opportunities
• Supportive work environment focused on health and well-being

Company Culture

• Diversity and Inclusion: We are committed to promoting a diverse workforce and include voices from all backgrounds.
• Empowerment: We empower our employees to take initiative and contribute to their work environment positively.
• Impactful Work: Our work directly influences patient care and outcomes and this motivates our team.