Clinical Research Associate

Job Description

As a Clinical Research Associate, you will play a key role in overseeing the conduct of clinical trials, ensuring compliance with regulatory standards and protocol adherence. You will work closely with investigators and study coordinators to monitor trial progress and maintain quality assurance throughout the study duration.

Responsibilities

• Conduct pre-study, interim, and close-out visits as required.
• Prepare monitoring visit reports according to regulatory standards.
• Engage in proactive problem-solving with clinical trial challenges.
• Maintain strict adherence to Good Clinical Practice (GCP) guidelines throughout the trial lifecycle.

Requirements

Education

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

Experience

• 4+ years within a clinical research role or similar

Technical Skills

• Clinical Data Management
• Risk Management

Soft Skills

• Problem Solving
• Team Collaboration

Languages

• English: Fluent

Advantageous

• Knowledge of medical terminology: Strong understanding of medical and therapeutic areas relevant to clinical trials.
• Background in biostatistics: Experience in applying statistical methods to clinical data.

Benefits

• Comprehensive health insurance coverage
• Generous annual leave and sick days
• Pension scheme with employer contributions
• Continued education support

Company Culture

• Commitment to Diversity: We actively promote a diverse workplace that respects and values individual contributions.
• Continuous Learning: We encourage ongoing education and provide pathways for personal growth.