
1001 - 5000 employees
Founded 1996
đ„ Healthcare
đŒ Consulting
đŠ Logistics
Healthcare âą Consulting âą Logistics
PSI CRO AG is a global contract research organization (CRO) that specializes in conducting clinical trials. The company focuses on delivering pivotal Phase 2 and 3 clinical trials across various therapeutic areas, including Inflammatory Bowel Diseases, Oncology, Hematology, Infectious Diseases, Multiple Sclerosis, and Rare Diseases. PSI utilizes a proprietary technology platform for clinical trial planning and financial tracking to ensure trials are conducted on time and within budget. The company is recognized for its expertise, quality, compatibility, and reliability, having been awarded the CRO Leadership Awards for multiple consecutive years.
đ„ 0 minutes ago
đ±đ» Latvia â Remote
â° Full Time
đą Junior
đĄ Mid-level
đ§Ș Clinical Research
đ» Ghost score 10%
Improve your chances of getting an interview by checking your resume score before you apply.

1001 - 5000 employees
Founded 1996
đ„ Healthcare
đŒ Consulting
đŠ Logistics
Healthcare âą Consulting âą Logistics
PSI CRO AG is a global contract research organization (CRO) that specializes in conducting clinical trials. The company focuses on delivering pivotal Phase 2 and 3 clinical trials across various therapeutic areas, including Inflammatory Bowel Diseases, Oncology, Hematology, Infectious Diseases, Multiple Sclerosis, and Rare Diseases. PSI utilizes a proprietary technology platform for clinical trial planning and financial tracking to ensure trials are conducted on time and within budget. The company is recognized for its expertise, quality, compatibility, and reliability, having been awarded the CRO Leadership Awards for multiple consecutive years.
âą Conduct and report all types of onsite monitoring visits âą Perform CRF review, source document verification and query resolution âą Be responsible for site communication and management âą Serve as a point of contact for in-house support services and vendors âą Communicate with internal project teams regarding study progress âą Participate in feasibility research âą Support the regulatory team in preparing documents for study submissions
âą College/University degree in Life Sciences or an equivalent combination of education, training & experience âą Independent monitoring experience in Latvia, preferably on contractor/freelance position âą Full working proficiency in English and Latvian âą Proficiency in MS Office applications âą Ability to plan, multitask and work in a dynamic team environment âą Communication, collaboration, and problem-solving skills âą Ability to travel âą Valid driver's license
âą Flexible working conditions âą Extensive training âą Opportunities for personal and professional growth âą Competitive salary agreed upon on an individual basis
Apply Now