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

📋 Description

• Execute and document various types of onsite monitoring visits.

• Conduct reviews of CRFs, verify source documents, and resolve queries.

• Oversee communication with sites.

• Manage study activities, timelines, and schedules for each site.

• Serve as the main point of contact for in-house support services and vendors.

• Assist in quality control efforts, including compliance monitoring and report evaluations.

• Develop and sustain relationships with clinical sites and investigators.

• Safeguard the rights, safety, and well-being of subjects while ensuring compliance with data quality standards.

⛳️ Requirements

• BSc or MSc in Life Sciences or a related field, or an equivalent combination of education, training, and experience.

• Experience with independent on-site monitoring in Slovakia.

• Proven experience in conducting all types of monitoring visits during Phase II and III trials.

• Proficiency in both Slovak and English.

• A valid driver's license and willingness to travel.

• Intermediate to advanced proficiency in MS Office.

• Strong communication, collaboration, and problem-solving abilities.

• Experience in supporting Oncology and Gastroenterology studies is an advantage.

🏝️ Benefits

• Opportunity for remote/home-based work within Slovakia.

• Support for professional development and career advancement.

• Guidance and assistance throughout the recruitment process.