About PSI CRO
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. PSIs global reach allows us to run clinical trials across multiple continents, in 50+ countries around the world. PSIs 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
458 Job openings in Psi Cro
Take your career to the next level and be involved in study startup processes in Trkiye. You will provide direct operational support to project teams and ensure that PSI clinical projects start smoothly and on time. Home-based or Office-BasedYou will:Support site identification a More...
Join our team of experts in regulatory and ethics submissions of clinical studies. You will focus on facilitating the start of research projects of novel medicinal products while taking a step further in your professional career.Office-based in TaipeiYour role:REGULATORY AFFAIRS More...
Were searching for a knowledgeable team-oriented Senior CRA to manage the clinical aspects of full-service global projects in Taiwan. As a Senior CRA at PSI you will work on the frontline of communication with project stakeholders ensuring the successful conduct of clinical trial More...
Were searching for a knowledgeable team-oriented CRA II to manage the clinical aspects of full-service global projects in Australia. As a CRA II at PSI you will work on the frontline of communication with project stakeholders ensuring timelines targets and standards of clini More...
Were searching for a knowledgeable team-oriented CRA II to manage the clinical aspects of full-service global projects in South Korea Seoul. As a CRA II at PSI you will work on the frontline of communication with project stakeholders ensuring timelines targets and standards More...
We are looking for a professional qualified and enthusiastic candidate to take up the full-time position of Receptionist/ Office Management Coordinator to support our well-established PSI Prague office.As the ideal candidate you have the ability to juggle multiple tasks and act as the More...
The Milestone One Site Coordinator role supports a Clinical Study Site in clinical trial related activities according to ICH-GCP protocol requirements within Study specific defined timelines and enrollment goals.This is a freelance part time assignment for around 05 FTEAct as the More...
The Milestone One Site Coordinator role supports a Clinical Study Site in clinical trial related activities according to ICH-GCP protocol requirements within Study specific defined timelines and enrollment goals.This is a freelance part time assignment for around 05 FTEAct as the More...
Take your career to the next level and be involved in study startup processes in Trkiye. You will provide direct operational support to project teams and ensure that PSI clinical projects start smoothly and on time. Based in Ankara Trkiye You will:Lead all study startup More...
The Milestone One Site Coordinator role supports a Clinical Study Site in clinical trial related activities according to ICH-GCP protocol requirements within Study specific defined timelines and enrollment goals.This is a freelance part time assignment for around 05 FTEAct as the More...
As a Senior CRA at PSI you will enjoy a variety of monitoring tasks and work on clinical studies in different therapeutic indications maintaining the highest quality standards in the industry.Office-based/Hybrid in Seoul South KoreaResponsibilitiesPrepare conduct and report site More...
Milestone One Site Coordinator supports trial sites in all related activities according to ICHGCP protocol requirements within Study specific defined timelines and enrollment goals.In this role you will:Act as the main line of communication between the Sponsor or CRO and the site More...
Take your career to the next level and be involved in study startup processes in Canada. You will provide direct operational support to project teams and ensure that PSI clinical projects start smoothly and on time. HybridYou will:Support site identification and selection process More...
Milestone One BD Representative supports our Business Development team in building and expanding the network of clients.In this role you will Build and sustain longlasting relationships with existing and potential clients (sponsors CROs medical institutions).Support
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Business Development Representative supports our Business Development team in building and expanding the Milestone One network as well promotes and supports attracting new projects for Milestone One network of sites.In this role you will Build and sustain long More...
This role supports our Business Development team in building and expanding the network of clients.In this role you will Build and sustain longlasting relationships with existing and potential clients (sponsors CROs medical institutions).Support Site Development Man More...
Milestone One BD Representative supports our Business Development team in building and expanding the network of clients.In this role you will Build and sustain longlasting relationships with existing and potential clients (sponsors CROs medical institutions).Support
 More...
Business Development Representative supports our Business Development team in building and expanding the network of clients.In this role you will Build and sustain longlasting relationships with existing and potential clients (sponsors CROs medical institutions).Support More...
As a Site Technology Specialist you will work with clinical trial sites to provide technical support and expertise related to imaging/radiology including radionuclide/radioligand therapy and cell therapy operations collectively referred to as technology.This position is based in Japa More...
Coordinates investigator/ site feasibility and identification process as well as study startup.Monitors project timelines and patient enrollment implements respective corrective and preventive measures.Reviews monitoring visit reports for all visit types and ensures reporting complian More...
