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 PSI as a Site Technology Specialist to support clinical trials with your expertise in dosimetry and medical physics.
Join PSI as a Clinical Research Associate II to conduct monitoring visits and manage clinical studies across various therapeutic areas.
We are seeking a Site Contract Specialist to support clinical research projects through contract negotiation and administrative activities.
The Senior Clinical Research Associate I will manage clinical research studies in Turkey, ensuring compliance and effective communication among stakeholders.
The Strategic Development Manager will lead the development and expansion of clinical operations in the UK and Ireland.
The Director of Business Oversight is responsible for managing client relationships and ensuring business interests are protected.
Join a dynamic global company as a Study Startup Specialist II, providing operational support for clinical projects in Turkey.
We are seeking a Director of Business Development to expand our client base in the United States and foster strong relationships within the healthcare sector.
Join PSI as a Senior Clinical Research Associate I to conduct monitoring visits and improve patients' lives.
Join Milestone One as a Clinical Trials Business Development Representative to expand their network and support clinical study sites.
Join PSI as a Clinical Research Associate II, managing clinical studies and ensuring compliance with industry standards.
The Site Contract Specialist I role involves negotiating site agreements and budgets in the clinical research industry.
Join PSI as a Medical Monitor specializing in Hematology, providing medical oversight for clinical studies and ensuring patient safety.
The Clinical Operations Manager will lead the team and manage clinical trials to ensure quality and compliance while building partnerships in the medical field.
The Lead Clinical Research Associate coordinates clinical trial activities and ensures compliance with regulatory standards while managing communication between project teams and trial sites.