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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.
We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together more than 3000 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.
