PSI CRO AG
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.
Number One Patient Enrollment CRO • Clinical Research • Clinical Trials • Oncology • Hematology
Senior Clinical Research Associate
16 hours ago
PSI CRO AG
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.
Number One Patient Enrollment CRO • Clinical Research • Clinical Trials • Oncology • Hematology
📋 Description
• Supervise study activities, timelines, milestones, and schedules on the country level. • Conduct and report all types of onsite monitoring visits. • Be involved in study set-up, including site contract and budget negotiations. • Ensure consistency of all study processes and identify country differences. • Responsible for execution and oversight of clinical trial country submissions and approvals for assigned protocols.
🎯 Requirements
• Bachelor's degree in Life Sciences, Pharmacy, or Registered Nursing; or an equivalent combination of education, training, and experience. • Minimum of 4-5 years of demonstrable, independent on-site monitoring experience or equivalent expertise. • Proficiency in feasibility assessment and study set-up processes is highly desirable. • Specialized experience in Oncology or Hematology therapeutic indications is a significant advantage. • Willingness and ability to travel extensively within Malaysia is a prerequisite for this position.
🏖️ Benefits
• Growth opportunities • Inspire your work with us • Collaborate with global teams • Access to cutting-edge treatments
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