About this role
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.