Clinical Research Coordinator

Job Description

We are seeking a Clinical Research Coordinator in Cambridge to manage and oversee clinical trials. The ideal candidate will ensure compliance with regulatory requirements while overseeing trial protocol and participant recruitment.

Responsibilities

• Develop and maintain study manuals and training materials.
• Ensure data integrity and confidentiality at all times.
• Assist in the preparation of grant applications and budgets.
• Conduct site visits to assess compliance and progress.
• Manage trial databases and electronic data capture systems.
• Prepare interim analysis for review by stakeholders.
• Implement strategies to enhance participant recruitment and retention.
• Collaborate with biostatisticians to ensure proper statistical methodology.
• Actively participate in team meetings and contribute to study design.
• Conduct literature reviews to inform trial protocols.

Requirements

Education

• Bachelor's degree in a relevant field
• Postgraduate qualification in Clinical Research preferred

Experience

• 3-5 years of experience in clinical trial management or coordination

Technical Skills

• Data Analysis
• Patient Interaction

Soft Skills

• Problem-solving
• Team Leadership

Certifications

• Certified Clinical Research Associate (CCRA)

Languages

• English: Fluent

Advantageous

• Experience in patient recruitment strategies: Knowledgeable in effective methods for recruiting trial participants.
• Understanding of pharmacovigilance principles: Awareness of drug safety monitoring and reporting practices.

Benefits

• Comprehensive health coverage and wellness programs
• Pension plan with employer contributions
• Flexible working arrangements
• Support for continuing education

Company Culture

• Continuous Improvement: We strive for continual improvement in our processes and outcomes.
• Diversity and Inclusion: We promote diversity and inclusivity in our workplace.
• Work-Life Balance: We support a healthy work-life balance for all employees.