Clinical Research Associate

About the role

We are seeking a motivated Clinical Research Associate to strengthen our clinical operations in Ukraine. The role combines remote and on‑site monitoring of clinical trials, ensuring compliance with international and local regulations while supporting high‑quality data collection.

Key responsibilities

• Monitor clinical trials to guarantee adherence to protocols, ICH‑GCP, SOPs and regulatory requirements.
• Conduct remote and on‑site visits, assess compliance, and manage documentation.
• Ensure data quality, integrity and patient safety throughout the study.
• Develop collaborative relationships with investigational sites and act as a site processes specialist.
• Facilitate communication between sponsors, regulatory authorities and trial sites, and maintain audit readiness.

Required profile

• Bachelor’s degree in life sciences or medical sciences.
• Minimum 4 years of on‑site monitoring experience.
• At least 2 years of hands‑on experience in Rheumatology and/or Oncology (advantageous).
• Strong ability to manage multiple projects and sites simultaneously.
• Fluent English (spoken and written) and a valid Category B driving licence.

Required skills

• ICH GCP knowledge.
• Clinical trial monitoring.
• Regulatory compliance.

What we offer

• Competitive salary.
• Flexible working hours with a home‑based option.
• Balanced workload focused on quality over quantity.
• Career growth in a continuous‑learning environment.
• Friendly, inclusive culture in an international privately‑owned company.
• Additional paid day off on your birthday.