Contract Clinical Research Associate

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

📋 Description

• Execute and document all varieties of onsite monitoring visits

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

• Oversee communication and management at the site level

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

• Interact with internal project teams regarding the progress of studies

• Engage in feasibility assessments

• Assist the regulatory team in preparing documentation for study submissions

⛳️ Requirements

• Bachelor’s degree in Life Sciences or an equivalent blend 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

• Competence in MS Office applications

• Capability to plan, juggle multiple tasks, and thrive in a dynamic team setting

• Strong communication, collaboration, and problem-solving abilities

• Willingness to travel

• Possession of a valid driver's license

🏝️ Benefits

• Flexible working arrangements

• Comprehensive training programs

• Opportunities for both personal and professional development

• Competitive salary