PSI CRO

We are seeking a highly independent and motivated Office All-Rounder to join our clinical research company as an integral part of our office operations. This position requires a full-time presence in the office and offers the opportunity to contribute to various aspects of office mana

We are seeking a highly independent and motivated Office All-Rounder to join our clinical research company as an integral part of our office operations. This position requires a full-time presence in the office and offers the opportunity to contribute to various aspects of office mana

We are seeking a professional qualified and enthusiastic candidate for a full-time IT Support Lead position. This role will involve providing support to junior administrators as well as delivering day-to-day technical support for our operations across Australia and the broader Asia Pa

We are seeking a professional qualified and enthusiastic candidate for a full-time IT Support Lead position. This role will involve providing support to junior administrators as well as delivering day-to-day technical support for our operations across Australia and the broader Asia Pa

We are looking for a Contract Budget Specialist to join the Project Finance team responsible for end-to-end management of budgeting processes for our projects conducted in the United States and Latin America. The person in this role will be a key financial partner for project teams si

We are looking for a Contract Budget Specialist to join the Project Finance team responsible for end-to-end management of budgeting processes for our projects conducted in the United States and Latin America. The person in this role will be a key financial partner for project teams si

In this role you will streamline activities of project teams and ensure consistency of Clinical Operations processes across Asia Pacific region. You will ensure meeting study milestones by project teams on a country level report study progress to clients and global stakeholders.The sc

In this role you will streamline activities of project teams and ensure consistency of Clinical Operations processes across Asia Pacific region. You will ensure meeting study milestones by project teams on a country level report study progress to clients and global stakeholders.The sc

This role is responsible for leading and supporting architectural fit-out and construction-related projects across PSIs office portfolio with primary focus on the USA and Canada regions. The position combines architectural planning project management contractor coordination and real e

This role is responsible for leading and supporting architectural fit-out and construction-related projects across PSIs office portfolio with primary focus on the USA and Canada regions. The position combines architectural planning project management contractor coordination and real e

1. Plans and executes assigned marketing campaigns (email social paid ads content PR internal communication)2. Creates content for assigned channels3. Tracks performance metrics and produces reports for stakeholders4. Analyzes performance of assigned campaigns and optimizes tactics5.

1. Plans and executes assigned marketing campaigns (email social paid ads content PR internal communication)2. Creates content for assigned channels3. Tracks performance metrics and produces reports for stakeholders4. Analyzes performance of assigned campaigns and optimizes tactics5.

Join our international team and support regulatory aspects of clinical research projects. Youll help streamline communication manage documents and maintain key systems - all while learning from experienced regulatory professionals.Office-Based in Bangalore IndiaWhat Youll Do:Communica

Join our international team and support regulatory aspects of clinical research projects. Youll help streamline communication manage documents and maintain key systems - all while learning from experienced regulatory professionals.Office-Based in Bangalore IndiaWhat Youll Do:Communica

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 in Kazakhstan while taking a step further in your professional career.Office-based in AlmatyYou will:Prepare cli

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 in Kazakhstan while taking a step further in your professional career.Office-based in AlmatyYou will:Prepare cli

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