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.
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:
We offer:
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.
Conducts clinical site monitoring and study oversight, managing site relationships, data quality, timelines, and regulatory support while protecting research participants’ rights, safety, and well-being.
Manage clinical trial activities across global projects, conducting site monitoring and supporting study startup while maintaining site relationships, patient safety, data quality, and compliance with study standards.
Conduct onsite and remote monitoring, manage site communications, and take ownership of assigned clinical studies across sponsors and therapeutic areas, supporting study quality and strong site relationships.
Oversee assigned clinical trial monitoring and site management, maintaining protocol and ICH GCP compliance, verifying source data, documenting site findings, and escalating issues.
Conduct onsite monitoring and support clinical study startup, site management, and study teams across therapeutic areas while maintaining high quality standards and supporting audits, inspections, and regulatory submissions.
