PSI CRO

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.Office-based in Tbilisi GeorgiaYou will:Conduct and report all types of onsi

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.Office-based in Tbilisi GeorgiaYou will:Conduct and report all types of onsi

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

In this role you will become the key support to clinical research projects streamlining communication with medical institutions maintaining systems and managing documents & information.Office-based in Tbilisi GeorgiaThe scope of responsibilities will include:Maintenance of databases a

In this role you will become the key support to clinical research projects streamlining communication with medical institutions maintaining systems and managing documents & information.Office-based in Tbilisi GeorgiaThe scope of responsibilities will include:Maintenance of databases a

Join our international team and be the key support to clinical research projects streamlining communication maintaining systems and managing documents & information. Only CVs in English will be accepted.You will be responsible for:Being the main point of contact between site personnel

Join our international team and be the key support to clinical research projects streamlining communication maintaining systems and managing documents & information. Only CVs in English will be accepted.You will be responsible for:Being the main point of contact between site personnel

We are looking for energetic proactive and enthusiastic candidates with multitasking skills and attention to detail to take up a full-time position of an Events Specialist in Tallinn.Full-time employment based in TallinnYou will:Prepare international events (travel will be rare and on

We are looking for energetic proactive and enthusiastic candidates with multitasking skills and attention to detail to take up a full-time position of an Events Specialist in Tallinn.Full-time employment based in TallinnYou will:Prepare international events (travel will be rare and on

Only CVs in English will be consideredWe are looking for a CRA to join our team in Mexico. Here you will have the opportunity to develop yourself as a senior trainer mentor and leader. We are committed to develop our employees in their careers by providing tailored courses and mentori

Only CVs in English will be consideredWe are looking for a CRA to join our team in Mexico. Here you will have the opportunity to develop yourself as a senior trainer mentor and leader. We are committed to develop our employees in their careers by providing tailored courses and mentori

Join our international team as a Coordinator Regional F&A where you will play a key role in ensuring accurate and timely out-of-pocket (OOP) expense reporting across the region. You will be able to take ownership of financial processes collaborate with cross-functional teams and contr

Join our international team as a Coordinator Regional F&A where you will play a key role in ensuring accurate and timely out-of-pocket (OOP) expense reporting across the region. You will be able to take ownership of financial processes collaborate with cross-functional teams and contr

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 a

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 a

As part of the PSI team you will have a fair degree of ownership and autonomy to make nuanced country-and department-specific adjustments while nurturing the global PSI culture that unites us across six continents. You will:Act as a specialized liaison to assist sites with a protocol-

As part of the PSI team you will have a fair degree of ownership and autonomy to make nuanced country-and department-specific adjustments while nurturing the global PSI culture that unites us across six continents. You will:Act as a specialized liaison to assist sites with a protocol-

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:

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

About the roleWe are looking for a Clinical Research Nurse to support the conduct of clinical trials through high-quality nursing care combined with clearly defined clinical research activities.In this role you will work under the supervision of the Director of Clinical Operations and

About the roleWe are looking for a Clinical Research Nurse to support the conduct of clinical trials through high-quality nursing care combined with clearly defined clinical research activities.In this role you will work under the supervision of the Director of Clinical Operations and

1. Study related activities (Laboratory Support). Manages all laboratory related activities within a clinical study under supervision including:Reviews laboratory-related study documentsProvides laboratory-related advice to PSI and Sponsor study teamsContributes to the development of

1. Study related activities (Laboratory Support). Manages all laboratory related activities within a clinical study under supervision including:Reviews laboratory-related study documentsProvides laboratory-related advice to PSI and Sponsor study teamsContributes to the development of

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

The Lead Site Coordinator (LSC) works as an integral part of the Operations team supporting clinical trial activities at assigned medical institutions. The LSC coordinates site-specific operational processes ensures smooth patient logistics assists with feasibility assessments and ser

The Lead Site Coordinator (LSC) works as an integral part of the Operations team supporting clinical trial activities at assigned medical institutions. The LSC coordinates site-specific operational processes ensures smooth patient logistics assists with feasibility assessments and ser

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 in Kyiv UkraineYour role will include:Liaising w

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 in Kyiv UkraineYour role will include:Liaising w

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.Full-time office-based in Tbilisi GeorgiaYour

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.Full-time office-based in Tbilisi GeorgiaYour

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.Your role:Prepare clinical trial documents for Regulator

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.Your role:Prepare clinical trial documents for Regulator

This role supports our Business Development team in building and expanding the sites network as well promotes and supports attracting new projects for Milestone One.In this role you will Build and sustain long-lasting relationships with Investigators and Medical Institutions represent

This role supports our Business Development team in building and expanding the sites network as well promotes and supports attracting new projects for Milestone One.In this role you will Build and sustain long-lasting relationships with Investigators and Medical Institutions represent

This role supports our Business Development team in building and expanding the sites network as well promotes and supports attracting new projects for Milestone One.In this role you will Build and sustain long-lasting relationships with Investigators and Medical Institutions represent

This role supports our Business Development team in building and expanding the sites network as well promotes and supports attracting new projects for Milestone One.In this role you will Build and sustain long-lasting relationships with Investigators and Medical Institutions represent