PSI is a leading Contract Research Organization with 30 years in the industry offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications.
1. Core responsibilities:
1.1. Provides administrative support to the Study Startup department with processes critical for site activation.
1.2. Supports Feasibility department with feasibility research and site identification activities.
1.3. Maintains project-specific tracking systems and electronic Trial Master File (eTMF) throughout the study startup phase.
1. Open to 2027 graduate majored in Life Science, Pharmaceutical, Medical or related.
2. Prior experience in clinical research is a plus.
3. Workable English in oral, written and reading.
4. Proficiency in standard Microsoft Office applications.
Make the right call and take your career to a whole new level. Join the company that focuses on its people and invests in their professional development and success.
PSI is a leading full-service global Contract Research Organization whose key strength is predictable patient enrollment across multiple therapeutic areas.
PSI is known in the industry as a CRO focused on ‘on-time project delivery’. This is achieved through investing substantial effort and MD resources into performing quality feasibility assessments that provide an accurate predictor of study timelines.
PSI’s global reach allows us to run clinical trials across multiple continents, in 50+ countries around the world.
PSI’s reputation is that of a 'no-nonsense' CRO focused on timely patient enrollment and project delivery. An exceptionally high repeat and referral business rates alongside low staff turnover are indicative of our commitment to be the best CRO in the world as measured by our clients and our employees.
http://www.psi-cro.com
