
1001 - 5000 employees
Founded 1996
🏥 Healthcare
💼 Consulting
📦 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.
🔥 12 hours ago
🗣️🇧🇷🇵🇹 Portuguese Required
Where this job comes from
Posted on PSI CRO AG's careers page, not through a job board
First seen by Remote Rocketship 12 hours ago
Still open on PSI CRO AG's site. Checked 17 minutes ago.

1001 - 5000 employees
Founded 1996
🏥 Healthcare
💼 Consulting
📦 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.
• Work on the frontline of communication with project stakeholders • Ensure timelines, targets and standards of clinical research projects • Build and maintain relationships with clinical sites and investigators • Focus on subjects’ rights, safety and well-being and quality of data compliance • Conduct and report all types of onsite monitoring visits • Participate in study startup • Perform CRF review, source document verification and query resolution • Manage site communication and management • Supervise study activities, timelines, and schedules on the country level • Serve as a point of contact for in-house support services and vendors • Participate in quality control, including compliance monitoring and report review • Participate in feasibility research • Support the regulatory team in preparing documents for study submissions
• College/University degree in Life Sciences or an equivalent combination of education, training & experience • A minimum of 1 year of independent on-site monitoring experience in Portugal • Experience in all types of monitoring visits in Phase II and/or III • Full working proficiency in English and Portuguese • 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
• Professional development and investment in career success • Home-based (freelance) work arrangement
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