PSI is a leading Contract Research Organization (CRO) with 30 years of experience in the pharmaceutical industry. Originated in Switzerland, PSI is a privately owned, full-service CRO with a global reach, supporting clinical trials across multiple countries and continents. Our reputation for being highly selective about the projects we undertake highlights our commitment to delivering high-quality, timely services across a broad spectrum of therapeutic indications.
At PSI, we foster an environment where a diverse range of colleagues feel welcomed and valued. Our inclusive culture is a cornerstone of our success, enabling us to attract and retain top talent globally.
We are not just about conducting clinical trials; we are about building a community where every team member has the opportunity to thrive and contribute to groundbreaking advancements in the pharmaceutical industry.
Clincial Data Manager plays a critical role in the clinical research project. If you are detail-oriented and committed to quality, able to work with large volume of clinical or medical data, you might be the professional we are looking for.
Please submit your CV in English
Based in Brazil
Responsibilities will include:
If you feel it is time to make your skills and knowledge visible within a growing company with true focus on its people, then PSI is the right choice for you.
At PSI, we foster an environment where a diverse range of colleagues feel welcomed and valued. Our inclusive culture is a cornerstone of our success, enabling us to attract and retain top talent globally.
The Clinical Data Manager is responsible for overseeing database management, ensuring data quality, and coordinating with project teams to support clinical trials.
The Clinical Data Manager is responsible for overseeing database setup, data entry, and ensuring the quality and integrity of clinical data throughout the research project.
As the Senior Director of Real World Data (RWD), you will define and implement RWD strategies and platforms to transform diverse datasets into regulatory-grade assets for clinical development and evidence generation.
Support clinical research projects by reviewing and negotiating site budgets and clinical trial agreements, while collaborating with various teams in a dynamic environment.
