Clinical Research Associate

Job Description

We are looking for a proactive Clinical Research Associate in Aberdeen to facilitate the successful delivery of clinical trials. The successful candidate will be responsible for monitoring study progress, collaborating with clinical teams, and maintaining study documentation.

Responsibilities

• Manage trial timelines and budgets effectively to ensure successful execution.
• Conduct data verification and quality control checks on study data.
• Prepare trial progress reports for internal and external stakeholders.
• Identify potential study risks and develop mitigation strategies.
• Maintain study supplies and equipment to ensure readiness for trials.
• Participate in site selection, initiation, and training.
• Assist in the preparation of study manuals, guidelines, and training materials.
• Support regulatory submissions and maintain records in compliance with applicable laws.

Requirements

Education

• Bachelor's degree in Life Sciences or related field
• Master's degree in a relevant field is an asset

Experience

• 2+ years of experience in clinical research or a similar role

Technical Skills

• Site Monitoring
• Regulatory Knowledge

Soft Skills

• Team Player
• Analytical Skills

Certifications

• Certified Clinical Research Associate (CCRA)

Languages

• English: Fluent

Advantageous

• Knowledge of statistical software: Experience with statistical analysis tools like SPSS or SAS.
• Clinical trial protocol writing: Experience in developing and writing clinical trial protocols.

Benefits

• Comprehensive health insurance
• Flexible working hours
• Employee assistance programme
• Work-life balance initiatives

Company Culture

• Diversity and Inclusion: We celebrate diversity and foster an inclusive workplace where everyone is respected.
• Community Impact: Our team is dedicated to making a positive impact in the community through our research.