Freelance Clinical Research Associate

EPM Scientific are currently partnered with a small Contract Research Organisation supporting international clinical research programs across Oncology and Cardiology. They are seeking a Freelance Clinical Research Associate to support ongoing clinical studies in Latvia. This position will play a key role in ensuring clinical trial activities are conducted in accordance with study protocols, ICH-GCP guidelines, and applicable regulatory requirements. See a summary of the role below:

Role Overview:

• Start date: November 2026
• Location: Latvia
• Contract Type: Freelance / Consultant - 0.3 FTE Contract
• Language: Latvian and English
• Project: Oncology and Cardiology Clinical Studies

Key Responsibilities:

• Conduct site monitoring activities including site initiation, routine monitoring, and close-out visits.
• Ensure investigator sites remain compliant with study protocols, ICH-GCP guidelines, and local regulations.
• Perform source data verification (SDV) and review clinical trial documentation for accuracy and completeness.
• Develop and maintain strong working relationships with investigators and site staff.
• Track and resolve site issues, protocol deviations, and data queries in a timely manner.
• Collaborate with Clinical Operations, Project Management, and sponsor teams to support study delivery and timelines.

Requirements:

• Bachelor's degree in Life Sciences, Pharmacy, Nursing, or a related scientific discipline.
• Previous experience as a Clinical Research Associate monitoring clinical trials.
• Experience within Oncology and/or Cardiology studies is strongly preferred.
• Solid understanding of clinical trial processes, ICH-GCP, and regulatory requirements.
• Fluency in Latvian and English.
• Strong organisational skills with the ability to work independently in a freelance capacity.
• Excellent communication and stakeholder management skills.

If this role is of interest to you, please apply directly to learn more. If not, feel free to share with your network.