Contract Clinical Research Associate

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

📋 Description

• Execute and document various onsite monitoring visits

• Conduct CRF assessments, source document verification, and resolve queries

• Manage communication and operations at the site

• Serve as a liaison for in-house support services and vendors

• Coordinate with internal project teams regarding study advancements

• Engage in feasibility assessments

• Assist the regulatory team in preparing documentation for study submissions

⛳️ Requirements

• Bachelor's degree in Life Sciences or an equivalent mix of education, training, and experience

• Experience in independent monitoring within Lithuania, ideally in a contractor or freelance capacity

• Full professional proficiency in both English and Lithuanian

• Knowledge of Latvian is an advantage

• Proficient in MS Office applications

• Capable of planning, multitasking, and thriving in a fast-paced team environment

• Strong communication, collaboration, and problem-solving skills

• Willingness to travel

• Valid driver's license

🏝️ Benefits

• Flexible working arrangements

• Comprehensive training opportunities

• Supportive team environment

• Potential for personal and professional development