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

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.
Originally posted on Himalayas