PSI CRO

Take your career to the next level and lead challenging full-service global clinical research projects managing the full scope of responsibilities and getting hands-on involvement in every aspect of the study.Based in ShanghaiYour responsibilities will include:Management of global mul

Take your career to the next level and lead challenging full-service global clinical research projects managing the full scope of responsibilities and getting hands-on involvement in every aspect of the study.Based in ShanghaiYour responsibilities will include:Management of global mul

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

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

Home-based position in São PauloOnly CVs in English will be consideredWe 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 employe

Home-based position in São PauloOnly CVs in English will be consideredWe 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 employe

If you are keen to provide administrative document management support to pharmaceutical research projects and be involved in something new outstanding and challenging this job opportunity is perfect for you!Only CVs in English will be considered.Responsibilities for this role include:

If you are keen to provide administrative document management support to pharmaceutical research projects and be involved in something new outstanding and challenging this job opportunity is perfect for you!Only CVs in English will be considered.Responsibilities for this role include:

At PSI Proposal Manager coordinates all phases of PSIs proposal process while maintaining the companys win rate of 30% and higher. You will contribute to everything from RFP strategy to bid defense slide decks. You will partner with global teams of subject matter experts from Feasibil

At PSI Proposal Manager coordinates all phases of PSIs proposal process while maintaining the companys win rate of 30% and higher. You will contribute to everything from RFP strategy to bid defense slide decks. You will partner with global teams of subject matter experts from Feasibil

At PSI Proposal Manager coordinates all phases of PSIs proposal process while maintaining the companys win rate of 30% and higher. You will contribute to everything from RFP strategy to bid defense slide decks.  You will partner with global teams of subject matter experts from Feasibi

At PSI Proposal Manager coordinates all phases of PSIs proposal process while maintaining the companys win rate of 30% and higher. You will contribute to everything from RFP strategy to bid defense slide decks.  You will partner with global teams of subject matter experts from Feasibi

At PSI Proposal Manager coordinates all phases of PSIs proposal process while maintaining the companys win rate of 30% and higher. You will contribute to everything from RFP strategy to bid defense slide decks.  You will partner with global teams of subject matter experts from Feasibi

At PSI Proposal Manager coordinates all phases of PSIs proposal process while maintaining the companys win rate of 30% and higher. You will contribute to everything from RFP strategy to bid defense slide decks.  You will partner with global teams of subject matter experts from Feasibi

Please submit your CV in English.You will contribute to statistical programming activities related to global clinical trials work closely with international teams of statisticians programmers and data managers program data sets and summaries.You will:Develop analysis data sets structu

Please submit your CV in English.You will contribute to statistical programming activities related to global clinical trials work closely with international teams of statisticians programmers and data managers program data sets and summaries.You will:Develop analysis data sets structu

Please submit your CV in English.You will contribute to statistical programming activities related to global clinical trials work closely with international teams of statisticians programmers and data managers program data sets and summaries.You will:Develop analysis data sets structu

Please submit your CV in English.You will contribute to statistical programming activities related to global clinical trials work closely with international teams of statisticians programmers and data managers program data sets and summaries.You will:Develop analysis data sets structu

Take your career to the next level and be involved in study startup processes in Türkiye. You will provide direct operational support to project teams ensure that clinical projects start smoothly and on time and support PSI in developing the local study startup team.Office-based in An

Take your career to the next level and be involved in study startup processes in Türkiye. You will provide direct operational support to project teams ensure that clinical projects start smoothly and on time and support PSI in developing the local study startup team.Office-based in An

The Site/Study Coordinator supports a medical institution in clinical trial-related activities. Protocol-specific tasks will be determined by the Principal Investigator considering all local and federal laws and regulations and upon review of competencies observed and documented by Mi

The Site/Study Coordinator supports a medical institution in clinical trial-related activities. Protocol-specific tasks will be determined by the Principal Investigator considering all local and federal laws and regulations and upon review of competencies observed and documented by Mi

PSI Medical Monitors provide medical input to global clinical studies and advise the teams and business partners while always focusing on patients safety and well-being.Home-Based in the United StatesResponsibilities:Advise clients project teams sites data safety monitoring boards reg

PSI Medical Monitors provide medical input to global clinical studies and advise the teams and business partners while always focusing on patients safety and well-being.Home-Based in the United StatesResponsibilities:Advise clients project teams sites data safety monitoring boards reg

PSI Medical Monitors provide medical input to global clinical studies and advise the teams and business partners while always focusing on patients safety and well-being.Home-Based in Canada.Responsibilities:Advise clients project teams sites data safety monitoring boards regulatory ag

PSI Medical Monitors provide medical input to global clinical studies and advise the teams and business partners while always focusing on patients safety and well-being.Home-Based in Canada.Responsibilities:Advise clients project teams sites data safety monitoring boards regulatory ag

 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 complia

 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 complia

Our global Process Improvement Department requires an Ontologist to fill the role of Associate Process Improvement within the Knowledge Management team. As an Associate Process Improvement at PSI you will be responsible for the following functions: Develop and maintain ontologies for

Our global Process Improvement Department requires an Ontologist to fill the role of Associate Process Improvement within the Knowledge Management team. As an Associate Process Improvement at PSI you will be responsible for the following functions: Develop and maintain ontologies for

Full-time employment in AustriaWere looking for a skilled IT Systems Engineer to manage and support Azure infrastructure with a focus on performance cost optimization and secure operations.Key ResponsibilitiesDeploy configure and maintain Azure resources including virtual machines sto

Full-time employment in AustriaWere looking for a skilled IT Systems Engineer to manage and support Azure infrastructure with a focus on performance cost optimization and secure operations.Key ResponsibilitiesDeploy configure and maintain Azure resources including virtual machines sto

Take your career to the next level and be involved in study startup processes in China. You will provide direct operational support to project teams and ensure that PSI clinical projects start smoothly and on time. Office-Based: ShanghaiYou will:Leads all study startup activities/proc

Take your career to the next level and be involved in study startup processes in China. You will provide direct operational support to project teams and ensure that PSI clinical projects start smoothly and on time. Office-Based: ShanghaiYou will:Leads all study startup activities/proc

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.Act as the main line of communication between the Sponsor or CRO and the

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.Act as the main line of communication between the Sponsor or CRO and the

Were looking for a skilled IT Systems Engineer to manage and support Azure infrastructure with a focus on performance cost optimization and secure operations.Key ResponsibilitiesDeploy configure and maintain Azure resources including virtual machines storage networking and security se

Were looking for a skilled IT Systems Engineer to manage and support Azure infrastructure with a focus on performance cost optimization and secure operations.Key ResponsibilitiesDeploy configure and maintain Azure resources including virtual machines storage networking and security se

Full-time employment in PragueWere looking for a skilled IT Systems Engineer to manage and support Azure infrastructure with a focus on performance cost optimization and secure operations.Key ResponsibilitiesDeploy configure and maintain Azure resources including virtual machines stor

Full-time employment in PragueWere looking for a skilled IT Systems Engineer to manage and support Azure infrastructure with a focus on performance cost optimization and secure operations.Key ResponsibilitiesDeploy configure and maintain Azure resources including virtual machines stor