Conducts site monitoring across clinical studies, ensuring protocol and regulatory compliance while overseeing recruitment, data quality, site risks, trial documentation, and investigator collaboration.
PSI CRO jobs
PSI is a leading full-service global CRO (Contract Research Organization).
74 open roles at PSI CRO
Clinical Research Associate II/ Senior Clinical Research Associate
Monitor clinical trials across therapeutic areas, ensuring site compliance, data quality, and participant safety while coordinating with investigators and project teams and mentoring less experienced associates.
Supports clinical research study start-up by negotiating site budgets and trial agreements, preparing and tracking contracts and grants, coordinating signatures, and maintaining trial documentation.
Manage and optimize COA/eCOA systems for clinical trials, coordinating licensing, translations, testing, deployment, integrations, vendor oversight, and ongoing support with study teams and stakeholders.
The Regional Project Lead is a senior clinical trial manager responsible for overseeing project teams, ensuring compliance with regulations, and meeting study milestones across designated countries.
The Regional Project Lead is a senior clinical trial manager responsible for overseeing project teams, ensuring compliance, and meeting study milestones across designated regions.
The Regional Project Lead is a senior clinical trial manager responsible for overseeing project teams across regions, ensuring compliance and meeting study milestones.
Lead and manage full-service clinical research projects in phase II and III, ensuring quality deliverables while mentoring project teams and supporting business development.
Lead full-service clinical research projects in phase II and III, managing responsibilities and ensuring quality deliverables on time and within budget.
Medical Monitor (US Board-Certified Gastroenterologist)
Provides medical oversight for global clinical trials, serving as the medical and safety contact, monitoring participant well-being, advising study teams, and contributing gastroenterology expertise throughout trial delivery.
Medical Monitor (Canada Board-Certified Gastroenterologist)
Provides medical oversight for global clinical trials, serving as the medical and safety contact, monitoring participant safety, reviewing trial data and documents, and advising teams on gastroenterology matters.
Coordinates laboratory support for clinical studies, helping sites with study setup, laboratory processes, documentation, training, and performance monitoring while connecting laboratories with sites and project teams.
Specialist Talent Acquisition - Temporary Contract
The Talent Acquisition Specialist will enhance the company's growth by managing end-to-end recruitment processes, ensuring a positive experience for candidates and hiring managers.
Specialist Talent Acquisition - Temporary Contract
The Talent Acquisition Specialist will lead end-to-end recruitment efforts across Europe, ensuring a positive experience for candidates and hiring managers in clinical trial operations.
Support clinical research projects by streamlining communication, maintaining systems, and managing documents to ensure project success.
Systems Engineer (Enterprise Applications Support)
Provide technical support for enterprise applications, troubleshoot issues, and participate in testing and implementation activities to ensure smooth business operations.
The Regional Project Lead is responsible for overseeing and coordinating clinical trial activities across regions, ensuring compliance with regulations and meeting study milestones.
The Lead Software Developer oversees software development projects, providing mentorship and technical guidance while architecting and maintaining applications to meet business needs.
Manage and optimize COA/eCOA systems for clinical trials, ensuring smooth integration and effective implementation to support project success.
Manage and optimize COA/eCOA systems for clinical trials, ensuring smooth integration and effective implementation to support project success.
As a Full Stack Developer, you will architect, develop, and maintain business applications while providing quality coding to support PSI's internal processes.
As a Full Stack Developer, you will architect, develop, and maintain business applications while providing quality coding to support PSI's internal processes and operations.
As a Full Stack Developer, you will architect, develop, and maintain business applications, providing quality coding to support PSI's internal processes and operations.
Study Startup Specialist II (18-months contract)
Coordinate clinical study startup in Australia by managing site activation milestones, budgets, regulatory documentation, submissions, timelines, and communication with project teams and investigational sites.
Page 1 · 74 results
