
PSI CRO is a prominent Contract Research Organization (CRO) with over 25 years of experience in the pharmaceutical industry. Founded in Switzerland, PSI is a privately owned, full-service CRO that operates globally, supporting clinical trials across various countries and continents. The company is known for its selective approach to project engagement, emphasizing high-quality and timely services across a wide range of therapeutic areas. PSI values diversity and inclusivity within its workforce, fostering an environment where all colleagues feel welcomed and valued. The organization is dedicated to not only conducting clinical trials but also building a community that empowers team members to thrive and contribute to significant advancements in the pharmaceutical sector.
Join Milestone One as a Manager Operations to lead and enhance global operational structures in clinical research.
Join Milestone One as a Manager Business Development to drive global expansion and build strategic relationships in clinical research.
The Marketing Director will lead a global marketing team and drive initiatives to enhance PSI's brand and market presence.
The Regional Site Partnership Associate is responsible for expanding Milestone One’s network of clinical research sites through strategic relationship development.
Join PSI as a Full Stack .NET Developer to architect and maintain business applications in a collaborative environment.
Manage clinical research operations and staff in a home-based role for the West Coast.
PSI is looking for a Legal Counsel to manage technology-related legal matters and ensure compliance with evolving regulations.
The Lead Clinical Research Associate will coordinate clinical research activities, ensuring compliance and managing project timelines.
Join PSI as a Study Startup Specialist I to support clinical project initiation processes from a home-based position in Canada.
We are seeking a Site Identification Specialist to develop strategic relationships with clinical research sites for clinical trials.
The RFI Coordinator at PSI is responsible for managing RFIs and supporting proposal efforts in a remote setting.
The Clinical Operations Manager will oversee staff and ensure quality in clinical research operations.
The Lead Clinical Research Associate oversees site monitoring and compliance for clinical trials while managing a team and ensuring data integrity.
The Document Specialist will manage documentation for pharmaceutical research projects, ensuring compliance and organization.
Join PSI as a Medical Monitor, providing critical medical input for clinical studies while working remotely in Canada.