
1001 - 5000 employees
Founded 1996
âïž Healthcare Insurance
đ Pharmaceuticals
đŹ Science
Healthcare Insurance âą Pharmaceuticals âą Science
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 April 24
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1001 - 5000 employees
Founded 1996
âïž Healthcare Insurance
đ Pharmaceuticals
đŹ Science
Healthcare Insurance âą Pharmaceuticals âą Science
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 Lead and facilitate initial and ongoing study Risk Management âą Participate in selection and setup of the RBM platform âą Perform Centralized Monitoring for a study âą Present Centralized Monitoring analysis results to study teams and clients âą Develop and review study-specific Plans âą Set up and manage targeted SDV and monitoring strategy for a study âą Set up and manage Central Data Review activities in a study âą Contribute to Proposals and bid defense meetings
âą College/University degree or an equivalent combination of education, training and experience âą Clinical Study Lead/Manager experience âą Strong communication & presentation skills âą Leadership and ability to work independently âą Centralized Monitoring experience is a plus âą Critical thinking and analytical skills âą Ability to work with complex data âą Ability to adapt to changing circumstances âą Knowledge of the process and functions in clinical trials âą Full working proficiency in English (Lithuanian proficiency is a plus) âą Proficiency in MS Office applications, Excel skills
âą Excellent working conditions âą Extensive training âą Friendly team âą Opportunities for personal and professional growth âą A fair and attractive salary and benefits package
Apply Nowđ April 4
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