Clinical Research Associate – Freelance

This is a fully remote position, open to applicants in Ireland.

📋 Description

• Conducting verification of data from source documents

• Performing site visits, which include pre-study, initiation, monitoring, and termination phases

• Ensuring compliance with all FDA, ICH-GCP, and local regulations

• Guaranteeing the implementation and adherence to FDA and ICH-GCP guidelines

• Engaging in budget negotiations and follow-up when necessary

• Assisting with data validation and resolving queries

• Providing mentorship to junior team members as needed

• Overseeing the collection and completion of regulatory documents

⛳️ Requirements

• At least 2 years of monitoring experience in oncology trials

• Experience in monitoring early-phase trials is a plus

• Possession of a Bachelor’s degree in a science-related field

• Exceptional understanding of medical terminology and the clinical monitoring process

• Strong knowledge of ICH-GCP guidelines

• Familiarity with clinical trial information systems

• Willingness to travel up to 60% on average

• Must have legal authorization to work in the country

🏝️ Benefits

• Competitive salary