Contract Clinical Research Associate

As a Clinical Research Associate at PSI you will enjoy a variety of monitoring tasks and work on clinical studies in different therapeutic indications, maintaining the highest quality standards in the industry.

Remote opportunity in Lithuania

You will:

• 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
• Be a point of contact for in-house support services and vendors
• Communicate with internal project teams regarding study progress
• Participate in feasibility research
• Support 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 Lithuania, preferably on contractor/freelance position
• Full working proficiency in English and Lithuanian
• Knowlegde of Latvian is a plus
• 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

We offer:

• Flexible working conditions
• Extensive training and friendly team
• Opportunities for personal and professional growth
• Competitive salary starting at 45 euro per hour. The precise salary depends on the specific qualifications and experience, and will be agreed upon on an individual basis.

If you feel it is time to make your skills and knowledge visible within a company with true focus on its people, then PSI CRO is the right choice for you.