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

📋 Description

• Initiate and activate sites for research projects.

• Maintain an in-depth understanding of assigned protocols.

• Assist with site initiation activities, including training, gathering essential documentation, and ensuring access to necessary systems.

• Prepare sites for monitoring in anticipation of the first subject's initial visit.

• Take responsibility for effective planning and execution of site recruitment.

• Keep regular communication with investigator sites.

• Ensure compliance with regulatory requirements, ICH-GCP standards, and protocol guidelines.

• Utilize judgment and experience to assess the overall performance of the site and its staff.

• Confirm that the informed consent process has been properly conducted.

• Record activities through follow-up letters, monitoring reports, communication logs, and other project documents as required by SOPs.

⛳️ Requirements

• At least 3 years of experience in Oncology clinical research.

• Proven experience managing Oncology protocols.

• Bachelor’s degree or RN in a relevant field, or an equivalent combination of education, training, and experience.

• Preferred proficiency in the local language; working proficiency in English is essential.

🏝️ Benefits

• Flexible working arrangements.