Full Time

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.Full-time office-based in Tbilisi Georgia You will:Conduct and report all ty

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.Full-time office-based in Tbilisi Georgia You will:Conduct and report all ty

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Full Time

Join our team of experts in regulatory 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 Prague the Czech RepublicYour role:Pr

Join our team of experts in regulatory 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 Prague the Czech RepublicYour role:Pr

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Full Time

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 computer systems

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 computer systems

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Full Time

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 Bangkok ThailandYou will:  Maintain upgrade and improve company IT infrastructure systems and networksDesign new computer s

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 Bangkok ThailandYou will:  Maintain upgrade and improve company IT infrastructure systems and networksDesign new computer s

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Full Time

If you are a qualified enthusiastic legal professional you may be the expert we are looking for to join our dynamic team in Ankara Türkiye.This role supports PSIs Legal with a primary focus on contracts related to clinical research. As an Associate Legal Counsel you will work closely

If you are a qualified enthusiastic legal professional you may be the expert we are looking for to join our dynamic team in Ankara Türkiye.This role supports PSIs Legal with a primary focus on contracts related to clinical research. As an Associate Legal Counsel you will work closely

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Were looking for an AI Engineer to join our growing Process Improvement team. If youre interested in AI solutions development and would like to further enhance your engineering skillset in a global company then PSI might be the right choice for you.Full-time office-based in Bangalore

Were looking for an AI Engineer to join our growing Process Improvement team. If youre interested in AI solutions development and would like to further enhance your engineering skillset in a global company then PSI might be the right choice for you.Full-time office-based in Bangalore

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Full Time

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 Taipei TaiwanYou will:  Maintain upgrade and improve company IT infrastructure systems and networksDesign new computer syst

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 Taipei TaiwanYou will:  Maintain upgrade and improve company IT infrastructure systems and networksDesign new computer syst

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Full Time

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.The function of the role may include but not limited to any/all of the fo

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.The function of the role may include but not limited to any/all of the fo

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Line manages assigned departmental staff (Clinical Research Associates)Interacts with other PSI departments on issues resolution and joint initiativesConducts performance appraisal and fosters professional development of departmental staffAdministratively supervises departmental staff

Line manages assigned departmental staff (Clinical Research Associates)Interacts with other PSI departments on issues resolution and joint initiativesConducts performance appraisal and fosters professional development of departmental staffAdministratively supervises departmental staff

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We are looking for professional qualified and enthusiastic candidates to take up a full-time position of a Junior IT Systems Administrator to provide daily technical support.The scope of responsibilities will include:Supervised responsibility for troubleshooting and diagnosing desktop

We are looking for professional qualified and enthusiastic candidates to take up a full-time position of a Junior IT Systems Administrator to provide daily technical support.The scope of responsibilities will include:Supervised responsibility for troubleshooting and diagnosing desktop

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Join our international team as a key support for clinical research this role you will streamline communication maintain systems and manage documents & information to support the success of our clinical research projects.This position is reserved for candidates belonging to protected

Join our international team as a key support for clinical research this role you will streamline communication maintain systems and manage documents & information to support the success of our clinical research projects.This position is reserved for candidates belonging to protected

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Full Time

Join our international team as a key support for clinical research projects. Your responsibilities will include:Maintain databases tracking systems and manage large volumes of documentsServe as the primary communication point for investigative sites and internal departmentsCoordinate

Join our international team as a key support for clinical research projects. Your responsibilities will include:Maintain databases tracking systems and manage large volumes of documentsServe as the primary communication point for investigative sites and internal departmentsCoordinate

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Full Time

In this role you will be involved in evaluation testing and implementation of IT infrastructure systems to support PSI business processes and operations.You will:  Maintain upgrade and improve company IT infrastructure systems and networksDesign new computer systems and frameworksMana

In this role you will be involved in evaluation testing and implementation of IT infrastructure systems to support PSI business processes and operations.You will:  Maintain upgrade and improve company IT infrastructure systems and networksDesign new computer systems and frameworksMana

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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 selec

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 selec

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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

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

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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:

Apply Now

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:

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Remote

We are looking for a Regulatory Officer to join our team in regulatory and ethics submissions of clinical studies in Mexico. You will focus on facilitating the start of research projects of novel medicinal products while taking a step further in your professional career.Only CVs in En

We are looking for a Regulatory Officer to join our team in regulatory and ethics submissions of clinical studies in Mexico. You will focus on facilitating the start of research projects of novel medicinal products while taking a step further in your professional career.Only CVs in En

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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:

Apply Now

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:

Apply Now