Clinical Research Coordinator

Job Description

We are seeking a detail-oriented Clinical Research Coordinator to join our Edinburgh team. You will be responsible for planning, conducting, and supervising clinical trials while maintaining compliance with protocols and regulations.

Responsibilities

• Manage participant enrollment and retention strategies.
• Ensure informed consent is obtained and documented appropriately.
• Coordinate lab work, scheduling, and sample collections.
• Facilitate data collection and manage databases.
• Develop patient education materials to promote understanding of trials.
• Implement risk management processes to enhance trial integrity.
• Provide support during audits and inspections.
• Foster a collaborative environment with research teams and external stakeholders.

Requirements

Education

• Bachelor's degree in a related field
• Advanced degree in Clinical Research or Medical Sciences is desirable

Experience

• 3+ years of experience in clinical research coordination or management

Technical Skills

• Project management
• Statistical analysis

Soft Skills

• Leadership
• Attention to detail

Certifications

• Certified Clinical Research Associate (CCRA)
• ISO 14155 certification

Languages

• English: Fluent

Advantageous

• Experience in multi-site study coordination: Ability to manage and coordinate studies across various locations.
• Familiarity with medical writing: Experience in developing clinical research documents.

Benefits

• Comprehensive health and wellness programs
• Retirement savings plan with employer contributions
• Work-life balance initiatives and remote work options
• Support for continuing education and career growth

Company Culture

• Continuous Learning: We value ongoing education and professional development.
• Integrity: We uphold high ethical standards in our research practices.
• Community Engagement: We actively participate in community initiatives and outreach.