Clinical Research Associate

Job Description

Join us as a Clinical Research Associate where you will support the execution of clinical trials. You will be involved in site selection, initiation, monitoring, and closure, ensuring quality and regulatory compliance throughout the process.

Responsibilities

• Conduct on-site monitoring to assess compliance with the trial protocol and relevant regulatory requirements.
• Review and validate source documents against clinical data.
• Identify issues and propose corrective actions to the study team.
• Facilitate communication among various departments involved in clinical trials.
• Maintain up-to-date knowledge on regulatory requirements and industry standards.
• Assist in the preparation for audits and inspections.
• Develop strong relationships with investigators and site staff to enhance collaboration.

Requirements

Education

• Bachelor's degree in Life Sciences or related field
• Master's degree is an advantage

Experience

• 2+ years of experience in a clinical trial setting

Technical Skills

• Regulatory Compliance
• Clinical Data Management

Soft Skills

• Problem-solving
• Teamwork

Certifications

• Certification in Clinical Research
• Good Clinical Practice Certification

Languages

• English: Fluent

Advantageous

• Knowledge of statistical analysis software: Experience in using tools for analyzing trial data.
• Familiarity with medical terminology: Understanding of medical language and concepts used in research.

Benefits

• Comprehensive medical insurance
• Retirement fund matching
• Generous leave policies
• Continuous training and development

Company Culture

• Excellence: We strive for excellence in every project and empower our employees to achieve their best.
• Supportive Environment: We foster a supportive culture where professional growth is encouraged.
• Diversity and Inclusion: We celebrate diversity and ensure everyone feels welcome and valued at our organization.