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

📋 Description

• Serve as a key point of communication with project stakeholders.

• Ensure adherence to timelines, objectives, and standards for clinical research projects.

• Establish and nurture relationships with clinical sites and investigators.

• Prioritize the rights, safety, and well-being of subjects, alongside ensuring data quality compliance.

• Conduct and document all varieties of onsite monitoring visits.

• Execute CRF reviews, source document verification, and resolution of queries.

• Oversee site communication and manage site-related activities.

• Supervise study timelines and schedules for each participating site.

• Act as the liaison for in-house support services and vendors.

• Assist in quality control through compliance monitoring and reviewing reports.

⛳️ Requirements

• Bachelor’s or Master’s degree in Life Sciences or a related field, or a combination of education, training, and experience.

• Proven independent on-site monitoring experience in Slovakia.

• Demonstrated expertise in various types of monitoring visits during Phase II and III studies.

• Proficiency in Slovak and English languages.

• Experience in supporting studies related to Oncology and Gastroenterology is advantageous.

• Possession of a valid driver's license and willingness to travel.

• Intermediate to advanced proficiency in MS Office applications.

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

🏝️ Benefits

• Opportunity for remote home-based work within Slovakia.

• Access to professional development and career support.

• Company commitment to investing in employees’ professional growth and success.

• Comprehensive recruitment guidance and support throughout the hiring process.