Clinical Data Reviewer

About the role

Join a global, fast‑growing team that focuses on smart, risk‑based monitoring of clinical studies. You will work remotely to ensure high‑quality study data, participant safety, and site performance.

Key responsibilities

• Review clinical data remotely, spotting errors, systemic issues and trends related to data integrity and site performance.
• Generate, follow up and resolve data queries, site issues and potential protocol deviations.
• Develop and maintain study‑specific Central Data Review tools, templates and tracking materials.
• Support the setup and management of risk‑based and central monitoring tools and activities.
• Assist with central monitoring signal review, root‑cause investigations and follow‑up.
• Provide the Central Monitoring Manager with study data, documents and reports.
• Contribute to inspection readiness, including eTMF quality control and study archive activities.

Required profile

• Bachelor’s degree.
• At least 1 year of experience in the clinical research industry.
• Clinical monitoring experience is a plus.
• English proficiency at CEFR B2 level or higher.
• Analytical mindset, strong attention to detail and ability to work in a dynamic team.

Required skills

• Proficiency in Microsoft Office applications (Word, Excel, PowerPoint).

What we offer

• Opportunities for professional development within a supportive, people‑focused company.
• Exposure to cutting‑edge medical science projects.