Contract Clinical Research Associate

Experience level: 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.

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.