Our client, a growing biotech client with a robust pipeline of assets targeting hard to treat cancers, are seeking an EU medical monitor to join their team.

Your responsibilities will include:

• Oversight of approximately 50 sites across Europe, ensuring proper conduct and compliance with the study protocol
• Ensure adherence to EMA regulations, GCP, and other relevant guidelines.
• Monitoring of data collection, entry, and validation processes to ensure accuracy and completeness
• Identification and mitigation of risks associated with clinical trials
• Reviewing protocol deviations
• Provision of training and support to clinical trial staff on regulatory requirements and study protocols
• Serving as a primary point of contact for clinical trial sites, investigators, and regulatory authorities.

Ideally you will have:

• A medical degree, preferably with specialisation in Oncology
• At least five years experience in a medical monitoring capacity
• Prior experience in working on a phase III study
• Excellent communication skills
• Proficiency in Spanish or Italian language would be advantageous