PSI CRO

In this role you will be responsible for managing and optimizing COA/eCOA systems for clinical trials. Your expertise will be vital in ensuring their smooth integration and effective implementation which will be key to the success of our projects.Full-time employment based in HungaryY

In this role you will be responsible for managing and optimizing COA/eCOA systems for clinical trials. Your expertise will be vital in ensuring their smooth integration and effective implementation which will be key to the success of our projects.Full-time employment based in HungaryY

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 clinical resear

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 clinical resear

Were searching for a knowledgeable team-oriented Senior CRA to manage the clinical aspects of full-service global projects in Australia. As a Senior CRA at PSI you will work on the frontline of communication with project stakeholders ensuring timelines targets and standards of clinica

Were searching for a knowledgeable team-oriented Senior CRA to manage the clinical aspects of full-service global projects in Australia. As a Senior CRA at PSI you will work on the frontline of communication with project stakeholders ensuring timelines targets and standards of clinica

We are looking for a Clinical Research Associate II to join a highly motivated international team where collaboration ownership and trust are part of everyday work.Hybrid role in MilanYou will:Conduct and report all types of onsite monitoring visits as well as remote visits.Perform CR

We are looking for a Clinical Research Associate II to join a highly motivated international team where collaboration ownership and trust are part of everyday work.Hybrid role in MilanYou will:Conduct and report all types of onsite monitoring visits as well as remote visits.Perform CR

Take your career to the next level and be involved in study startup processes in Italy. You will provide direct operational support to project teams and ensure that PSI clinical projects start smoothly and on time. This role is hybrid in our Milan officeYou will:Support site identific

Take your career to the next level and be involved in study startup processes in Italy. You will provide direct operational support to project teams and ensure that PSI clinical projects start smoothly and on time. This role is hybrid in our Milan officeYou will:Support site identific

Take your career to the next level and be involved in Study Startup processes in Israel. You will provide direct operational support to project teams and ensure that PSI clinical projects start smoothly and on time. You will:Manage Startup activities and metrics while planning sites a

Take your career to the next level and be involved in Study Startup processes in Israel. You will provide direct operational support to project teams and ensure that PSI clinical projects start smoothly and on time. You will:Manage Startup activities and metrics while planning sites a

This position requires relocation to Trebinje area in Bosnia and Herzegovina.As a Clinical Research Associate 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

This position requires relocation to Trebinje area in Bosnia and Herzegovina.As a Clinical Research Associate 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

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.Hybrid working arrangement in Milan areaYour role:Suppor

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.Hybrid working arrangement in Milan areaYour role:Suppor

As a Senior CRA you will work on the frontline of communication with project stakeholders ensuring timelines targets and standards of clinical research projects in a variety of therapeutic indications. You will build and maintain relationships with clinical sites and investigators. Yo

As a Senior CRA you will work on the frontline of communication with project stakeholders ensuring timelines targets and standards of clinical research projects in a variety of therapeutic indications. You will build and maintain relationships with clinical sites and investigators. Yo

As a Clinical Research Associate II you will work on the frontline of communication with project stakeholders ensuring timelines targets and standards of clinical research projects in a variety of therapeutic indications.  You will build and maintain relationships with clinical sites

As a Clinical Research Associate II you will work on the frontline of communication with project stakeholders ensuring timelines targets and standards of clinical research projects in a variety of therapeutic indications.  You will build and maintain relationships with clinical sites

Milestone One Site Coordinator supports trial sites in all related activities according to ICH-GCP 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.Ens

Milestone One Site Coordinator supports trial sites in all related activities according to ICH-GCP 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.Ens

As a Clinical Research Associate 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.You will:Conduct and report all types of onsite monitoring visitsBe involved

As a Clinical Research Associate 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.You will:Conduct and report all types of onsite monitoring visitsBe involved

This is an excellent opportunity to build broad clinical operations experience working directly with investigative sites and international project teams with opportunities to develop further within clinical research.The scope of responsibilities will include:Serve as a key point of co

This is an excellent opportunity to build broad clinical operations experience working directly with investigative sites and international project teams with opportunities to develop further within clinical research.The scope of responsibilities will include:Serve as a key point of co

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 positionYour role:Prepare clinical trial s

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 positionYour role:Prepare clinical trial s

As a Clinical Research Associate 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.You will:Conduct and report SIV RMV COV onsite monitoring visitsPerform CRF

As a Clinical Research Associate 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.You will:Conduct and report SIV RMV COV onsite monitoring visitsPerform CRF

Please submit your CV in EnglishWe are looking for experienced candidates to fill the Project Finance Manager position and to be involved in clinical project budgeting negotiating and analyzing budgets as well as providing support with proposals and contract management activities with

Please submit your CV in EnglishWe are looking for experienced candidates to fill the Project Finance Manager position and to be involved in clinical project budgeting negotiating and analyzing budgets as well as providing support with proposals and contract management activities with

We are looking for experienced candidates to fill the Project Finance Manager position and to be involved in clinical project budgeting negotiating and analyzing budgets as well as providing support with proposals and contract management activities within the company.Onsite in Tbilisi

We are looking for experienced candidates to fill the Project Finance Manager position and to be involved in clinical project budgeting negotiating and analyzing budgets as well as providing support with proposals and contract management activities within the company.Onsite in Tbilisi

We are looking for experienced candidates to fill the Project Finance Manager position and to be involved in clinical project budgeting negotiating and analyzing budgets as well as providing support with proposals and contract management activities within the company.Hybrid in Oxford

We are looking for experienced candidates to fill the Project Finance Manager position and to be involved in clinical project budgeting negotiating and analyzing budgets as well as providing support with proposals and contract management activities within the company.Hybrid in Oxford

PSI CRO is looking for an experienced project finance professional in the Clinical Research industry who will be responsible for creating managing negotiating and analyzing clinical project budgets as well as providing support with proposals and contract management activities within t

PSI CRO is looking for an experienced project finance professional in the Clinical Research industry who will be responsible for creating managing negotiating and analyzing clinical project budgets as well as providing support with proposals and contract management activities within t

We are looking for experienced candidates to fill the Project Finance Manager position and to be involved in clinical project budgeting negotiating and analyzing budgets as well as providing support with proposals and contract management activities within the company.Responsibilities:

We are looking for experienced candidates to fill the Project Finance Manager position and to be involved in clinical project budgeting negotiating and analyzing budgets as well as providing support with proposals and contract management activities within the company.Responsibilities: