- Provide medical input to global clinical studies and advise teams and business partners, focusing on patients' safety and well-being.
- Collaborate with internal departments in preparing clinical development plans, protocols, investigator brochures, and clinical study reports.
- Review and analyze clinical data to ensure the safety of study participants and ensure data accuracy and trial compliance.
PSI is a leading Contract Research Organization (CRO) with 30 years of experience in the pharmaceutical industry. They're a privately owned, full-service CRO with a global reach, supporting clinical trials across multiple countries, committed to delivering high-quality, timely services. PSI fosters an environment where a diverse range of colleagues feel welcomed and valued, enabling them to attract and retain top talent globally and build a community where every team member has the opportunity to thrive.