Clinical Research Associate

Job Description

We're on the lookout for a detail-oriented Clinical Research Associate to join our Aberdeen team. This role involves overseeing clinical trials, ensuring compliance with regulatory standards, and collaborating closely with investigators and clinical staff.

Responsibilities

• Plan and manage the execution of clinical trials from start to finish.
• Conduct follow-up meetings with investigators and site staff.
• Ensure site compliance with company policies and GCP guidelines.
• Coordinate logistics for trial supplies and manage inventory.
• Maintaining a positive and engaging relationship with site personnel.
• Participate in training sessions to enhance knowledge on clinical research.
• Assist in the preparation of meeting materials and presentations.
• Evaluate site performance and implement corrective actions as needed.

Requirements

Education

• Bachelor's degree in a related field
• Master's degree in Clinical Research is preferred

Experience

• 3+ years of experience in clinical research monitoring

Technical Skills

• Site Monitoring
• Protocol Development

Soft Skills

• Teamwork
• Analytical Thinking

Certifications

• Society of Clinical Research Associates (SoCRA) Certification
• Clinical Research Associate (CRA) Certification

Languages

• English: Fluent

Advantageous

• Experience with statistical software: Familiarity with software such as SPSS or SAS for data analysis.
• Previous experience in a clinical trial project lead role: Experience overseeing clinical trials as a project lead.

Benefits

• Annual performance bonus
• Flexible working hours
• Professional development programs
• Access to wellness programs and resources

Company Culture

• Diversity and Inclusion: We celebrate diversity and inclusion in our workplace.
• Work-Life Balance: We promote a healthy work-life balance for all employees.
• Continuous Improvement: We are committed to continuous improvement and professional development.