
1001 - 5000 employees
Founded 1996
đĽ Healthcare
đź Consulting
đŚ Logistics
Healthcare ⢠Consulting ⢠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.
đĽ 1 hour ago
đŹđ§ United Kingdom â Remote
â° Full Time
đ˘ Junior
đĄ Mid-level
đ§Ş Clinical Research
đť Ghost score 10%
Where this job comes from
Posted on PSI CRO AG's careers page, not through a job board
First seen by Remote Rocketship 1 hour ago

1001 - 5000 employees
Founded 1996
đĽ Healthcare
đź Consulting
đŚ Logistics
Healthcare ⢠Consulting ⢠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.
⢠Conduct and report all types of onsite monitoring visits ⢠Be involved in study startup, if applicable ⢠Perform CRF review, source document verification and query resolution ⢠Be responsible for site communication and management ⢠Serve as a point of contact for in-house support services and vendors ⢠Communicate with internal project teams regarding study progress ⢠Participate in feasibility research ⢠Support the regulatory team in preparing documents for study submissions ⢠Build and maintain relationships with clinical sites and investigators ⢠Focus on subjects' rights, safety and well-being and quality of data compliance
⢠College/University degree in Life Sciences or an equivalent combination of education, training & experience ⢠Clinical Research or Medical experience ⢠Independent on-site monitoring experience in the UK ⢠PC skills to be able to work with MS Word, Excel and PowerPoint ⢠Ability to plan, multitask and work in a dynamic team environment ⢠Communication, collaboration, and problem-solving skills ⢠Ability to travel ⢠Valid driver's license
⢠Employees can work remotely ⢠Support of a knowledgeable and professional team ⢠Opportunity to develop a variety of skills while progressing with the company ⢠Contribution to full-scale challenging projects
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