Contract Clinical Research Associate

• Conduct and report all types of onsite monitoring visits
• Perform CRF review, source document verification and query resolution
• Be responsible for site communication and management
• Serve as a point of contact for in-house support services and vendors
• Communicate with internal project teams regarding study progress
• Participate in feasibility research
• Support the regulatory team in preparing documents for study submissions

• College/University degree in Life Sciences or an equivalent combination of education, training & experience
• Independent monitoring experience in Latvia, preferably on contractor/freelance position
• Full working proficiency in English and Latvian
• Proficiency in MS Office applications
• Ability to plan, multitask and work in a dynamic team environment
• Communication, collaboration, and problem-solving skills
• Ability to travel
• Valid driver's license

• Flexible working conditions
• Extensive training
• Opportunities for personal and professional growth
• Competitive salary agreed upon on an individual basis