PSI CRO

Join our global Talent Acquisition team and play a key role in growing the company across a variety of functions supporting clinical trial operations. The Talent Acquisition Specialist is responsible for delivering end-to-end recruitment across Europe ensuring an outstanding experienc

Join our global Talent Acquisition team and play a key role in growing the company across a variety of functions supporting clinical trial operations. The Talent Acquisition Specialist is responsible for delivering end-to-end recruitment across Europe ensuring an outstanding experienc

Join our global Talent Acquisition team and play a key role in growing the company across a variety of functions supporting clinical trial operations. The Talent Acquisition Specialist is responsible for delivering end-to-end recruitment across Europe ensuring an outstanding experienc

Join our global Talent Acquisition team and play a key role in growing the company across a variety of functions supporting clinical trial operations. The Talent Acquisition Specialist is responsible for delivering end-to-end recruitment across Europe ensuring an outstanding experienc

Join our international team and be the key support to clinical research projects streamlining communication maintaining systems and managing documents & information. You will focus on facilitating research projects of novel medicinal products while taking a step further in your profes

Join our international team and be the key support to clinical research projects streamlining communication maintaining systems and managing documents & information. You will focus on facilitating research projects of novel medicinal products while taking a step further in your profes

With the industry moving forward the central monitoring function has become a top priority at PSI. We are looking for a person who would lead the risk-based monitoring approach implementation on the clinical study and program level to ensure patient safety and data integrity.You will:

With the industry moving forward the central monitoring function has become a top priority at PSI. We are looking for a person who would lead the risk-based monitoring approach implementation on the clinical study and program level to ensure patient safety and data integrity.You will:

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 developing your professional career.Hybrid working arrangement in Prague the Czec

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 developing your professional career.Hybrid working arrangement in Prague the Czec

With the industry moving forward the central monitoring function has become a top priority at PSI. We are looking for a person who would lead the risk-based monitoring approach implementation on the clinical study and program level to ensure patient safety and data integrity.You will:

With the industry moving forward the central monitoring function has become a top priority at PSI. We are looking for a person who would lead the risk-based monitoring approach implementation on the clinical study and program level to ensure patient safety and data integrity.You will:

With the industry moving forward the central monitoring function has become a top priority at PSI. We are looking for a person who would lead the risk-based monitoring approach implementation on the clinical study and program level to ensure patient safety and data integrity.You will:

With the industry moving forward the central monitoring function has become a top priority at PSI. We are looking for a person who would lead the risk-based monitoring approach implementation on the clinical study and program level to ensure patient safety and data integrity.You will:

With the industry moving forward the central monitoring function has become a top priority at PSI. We are looking for a person who would lead the risk-based monitoring approach implementation on the clinical study and program level to ensure patient safety and data integrity.You will:

With the industry moving forward the central monitoring function has become a top priority at PSI. We are looking for a person who would lead the risk-based monitoring approach implementation on the clinical study and program level to ensure patient safety and data integrity.You will:

We are looking for a motivated clinical research professional to join our team and support the successful start-up of clinical studies in this role you will work closely with project teams and investigational sites coordinating activities from site contracts and regulatory documentat

We are looking for a motivated clinical research professional to join our team and support the successful start-up of clinical studies in this role you will work closely with project teams and investigational sites coordinating activities from site contracts and regulatory documentat

Business Development Manager supports our Business Development team in building and expanding the network of clients.In this role you will Build and sustain long-lasting relationships with existing and potential clients (sponsors CROs medical institutions).Support Site Development Man

Business Development Manager supports our Business Development team in building and expanding the network of clients.In this role you will Build and sustain long-lasting relationships with existing and potential clients (sponsors CROs medical institutions).Support Site Development Man

As a Clinical Research Associate II 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 invol

As a Clinical Research Associate II 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 invol

We looking for a knowledgeable proactive and self-motivated Systems Engineer to join our global yet closely-knit Systems Development team. Our in-house projects include but are not limited to web and desktop apps ERP system BPM system document management system AI initiatives and more

We looking for a knowledgeable proactive and self-motivated Systems Engineer to join our global yet closely-knit Systems Development team. Our in-house projects include but are not limited to web and desktop apps ERP system BPM system document management system AI initiatives and 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 trials in

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 trials in

As a Clinical Research Associate I 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 a

As a Clinical Research Associate I 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 a

Official job title will be Site Contract Specialist I and can be based anywhere in Canada. The core responsibilities of this role include:Facilitating negotiations of site agreements and budgets to ensure alignment with the site activation plan Customizing and preparing country- and s

Official job title will be Site Contract Specialist I and can be based anywhere in Canada. The core responsibilities of this role include:Facilitating negotiations of site agreements and budgets to ensure alignment with the site activation plan Customizing and preparing country- and s

Full-time employment based in LatviaYou will:Provide support of off-the shelf software packages (Tier 2 and Tier 3)Perform installation of Tier 3 and certain Tier 4 information systems and conduct user trainingPerform installation and support of specialized systems (e.g. special wareh

Full-time employment based in LatviaYou will:Provide support of off-the shelf software packages (Tier 2 and Tier 3)Perform installation of Tier 3 and certain Tier 4 information systems and conduct user trainingPerform installation and support of specialized systems (e.g. special wareh

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.Remote opportunity in LatviaApprox. 0.5 FTEYou will:Conduct and report all t

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.Remote opportunity in LatviaApprox. 0.5 FTEYou will:Conduct and report all t

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 Mexico.Only CVs in English

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 Mexico.Only CVs in English

We looking for a knowledgeable proactive and self-motivated Systems Engineer to join our global yet closely-knit Systems Development team. Our in-house projects include but are not limited to web and desktop apps ERP system BPM system document management system AI initiatives and more

We looking for a knowledgeable proactive and self-motivated Systems Engineer to join our global yet closely-knit Systems Development team. Our in-house projects include but are not limited to web and desktop apps ERP system BPM system document management system AI initiatives and 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 Argentina.Only CVs in Engli

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 Argentina.Only CVs in Engli