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

Qualifications :

• 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 drivers license

Additional Information :

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.

Remote Work :

Yes

Employment Type :

Full-time