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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
501 Job openings in Psi Cro
In this role you will be involved in evaluation testing and implementation of IT infrastructure systems to support PSI business processes and operations.Based in Seoul South KoreaYou will: Maintain upgrade and improve company IT infrastructure systems and networksDesign new More...
In this role you will be involved in evaluation testing and implementation of IT infrastructure systems to support PSI business processes and operations.Based in SingaporeYou will: Maintain upgrade and improve company IT infrastructure systems and networksDesign new compute More...
The Executive Assistant provides high-level assistance to Head of Asia and Director of Clinical Operations in Australia and Taiwan. This new and unique opportunity allows you to be part of PSI in the development of clinical drugs by enhancing the productivity of our leadership th More...
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...
Assesses feasibility of research protocols based on knowledge and experience and in accordance with designated criteria to select the most suitable studies for the clinical site. Supervises the conduct of clinical trials in accordance with ICH GCP applicable regulations pro More...
Assesses feasibility of research protocols based on knowledge and experience and in accordance with designated criteria to select the most suitable studies for the clinical site. Supervises the conduct of clinical trials in accordance with ICH GCP applicable regulations pro More...
We are looking for an experienced CRA ready to train and coordinate junior CRAs on site. Here you will have the opportunity to develop yourself as a trainer mentor and leader. We are committed to develop our employees in their careers by providing tailored courses and mentoring.Respon More...
Were hiring a M365 IT Administrator to help manage maintain and enhance our Microsoft 365 ecosystemincluding Exchange Online SharePoint Online Teams OneDrive Intune Power Platform and Microsoft Security & Compliance solutions.Youll play a key role in ensuring our environment More...
Were searching for a knowledgeable team-oriented Senior CRA to manage the clinical aspects of full-service global projects in Malaysia. As a Senior CRA at PSI you will work on the frontline of communication with project stakeholders ensuring the successful conduct of clinical tri More...
Join our LatAm team to be the key support to clinical research projects as part of the start-up team. You will work in a dynamic multi-functional environment gaining unique skills from various disciplines relevant to clinical research.Home-based position in Brazil. More...
We are now expanding Operations and looking for a dynamic and knowledgeable Coordinator to join PSI Grants Expense Management division.Based in Tbilisi GeorgiaIn this role your goal will be to ensure that physicians and hospitals receive on time and accurate payments for the More...
As a Regulatory Officer will work closely with our global team of experts to prepare clinical trial dossiers for regulatory and authorities deliver regulatory training to project teams and communicate with stakeholders on regulatory-related matters. Join PSI and help drive innovation More...
Preparation conduct and reporting of selection initiation routine and closeout monitoring visitsSite management general administration of clinical research studies in TurkeyContact for clinical investigators vendors and support services in regard to study progressMonitoring trial prog 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...
Join our international team and be the key support to clinical research projects as part of the start-up team working in a dynamic multi-functional environment gaining unique skills from various disciplines relevant to clinical research.Office-based or remote in TrkiyeYou will:Co 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. Home-based or Office-BasedYou will:Support site identification a More...
As a Senior Clinical Research Associate I 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.Hybrid work in AlmatyYou will:Conduct and report
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Preparation conduct and reporting of selection initiation routine and closeout monitoring visitsSite management general administration of clinical research studies in TurkeyContact for clinical investigators vendors and support services in regard to study progressMonitoring trial prog More...
Join our international team and be the key support to clinical research projects in Trkiye streamlining communication maintaining systems and managing documents & information.Site ManagementExchanges data documents and other project relevant information between investigative More...
The Strategic Development Manager will work closely with Country Management to support the development and expansion of UK & Ireland operations and assist in the set up of Milestone One. Some of the activities conducted by the SDM include;Communication of recommendations for devel More...