is part of a group of Animal Health Contract Research Organisations servicing the general animal health industry.
Field Clinical Trials
This role provides the flexibility to work remotely, with occasional visits to Clinaxel offices based in the North of France.
Responsible for performing monitoring activities to ensure clinical trials are conducted in compliance with study protocols, VICH GL9 GCP guidelines, and applicable regulatory requirements. This role involves verifying data accuracy, ensuring site adherence to timelines and quality standards, and supporting the overall success of clinical trials.
Conduct routine site monitoring visits across all trial phases to ensure compliance with study protocols, GCP guidelines, and regulatory requirements.
Verify the accuracy and completeness of data collected at study sites, identifying and resolving discrepancies as needed.
Assist in the preparation and review of study-related documentation, including monitoring reports and site records.
Ensure site adherence to established timelines, quality standards, and budgetary constraints.




Document and escalate risks or issues that may impact study timelines or data quality to the appropriate stakeholders.
Qualification, Training and Experience Requirements
Bachelor's degree in a relevant Life Sciences field.
Minimum of two years' experience in GCP Study Monitoring within Animal Health or Human Pharma sectors.
Ability to work and communicate in English.
This is a remote position, with the potential for regular travel based on project requirements.
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The Company complies with local and international data protection and privacy legislation. By applying for this position, applicants agree to the processing of their personal data in accordance with our recruitment procedure and Privacy Notice available from our website. Personal data will be used solely for recruitment purposes and handled with strict confidentiality.

📌 Monitor/a (remote) (Málaga)
🏢 Clinglobal Group
📍 Málaga