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 Latvia Approx. 0.5 FTE 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 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 We offer: • Flexible working conditions • Extensive training and friendly team • Opportunities for personal and professional growth • Competitive salary 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.