About The Position

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

Requirements

  • 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
  • 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

Nice To Haves

  • Knowledge of Latvian is a plus

Responsibilities

  • 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

Benefits

  • Flexible working conditions
  • Extensive training and friendly team
  • Opportunities for personal and professional growth
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