PSI CRO

Take your career to the next level and lead challenging study activation process on a country level. You will support clinical research teams and ensure PSI projects start smoothly and on time.You will mainly: Lead finalization of site/vendor agreements and budgets negotiation to ensu

Take your career to the next level and lead challenging study activation process on a country level. You will support clinical research teams and ensure PSI projects start smoothly and on time.You will mainly: Lead finalization of site/vendor agreements and budgets negotiation to ensu

 SCOPE OF RESPONSIBILITIES1. Office Management1.1. Responsible for new office site selection decoration vendor management and etc.1.2. Coordinates the purchase and inventory of office supplies1.3. Oversees office maintenance and management of the office vendors to ensure smooth operat

 SCOPE OF RESPONSIBILITIES1. Office Management1.1. Responsible for new office site selection decoration vendor management and etc.1.2. Coordinates the purchase and inventory of office supplies1.3. Oversees office maintenance and management of the office vendors to ensure smooth operat

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 role in Raanana  IsraelYou 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 while taking a step further in your professional career.Office-based role in Raanana  IsraelYou will:Prepare cli

Join our international team and be the key support to clinical research projects streamlining communication maintaining systems and managing documents & information.The scope of responsibilities will include:Maintenance of databases and tracking systemsServes as the primary sites cont

Join our international team and be the key support to clinical research projects streamlining communication maintaining systems and managing documents & information.The scope of responsibilities will include:Maintenance of databases and tracking systemsServes as the primary sites cont

Take your career to the next level and lead challenging study activation process on a country level. You will support clinical research teams and ensure PSI projects start smoothly and on time.You will mainly: Lead finalization of site/vendor agreements and budgets negotiation to ensu

Take your career to the next level and lead challenging study activation process on a country level. You will support clinical research teams and ensure PSI projects start smoothly and on time.You will mainly: Lead finalization of site/vendor agreements and budgets negotiation to ensu

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:Act as the main line of communication between the project team spon

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:Act as the main line of communication between the project team spon

PSI Medical Monitors provide medical input to global clinical studies and advise the teams and business partners while always focusing on patients safety and well-being.Responsibilities:Advise clients project teams sites regulatory agencies and third-party vendors on medical mattersCo

PSI Medical Monitors provide medical input to global clinical studies and advise the teams and business partners while always focusing on patients safety and well-being.Responsibilities:Advise clients project teams sites regulatory agencies and third-party vendors on medical mattersCo

PSI Medical Monitors provide medical input to global clinical studies and advise the teams and business partners while always focusing on patients safety and well-being.Full-time employment based in PolandResponsibilities:Advise clients project teams sites regulatory agencies and thir

PSI Medical Monitors provide medical input to global clinical studies and advise the teams and business partners while always focusing on patients safety and well-being.Full-time employment based in PolandResponsibilities:Advise clients project teams sites regulatory agencies and thir

PSI Medical Monitors provide medical input to global clinical studies and advise the teams and business partners while always focusing on patients safety and well-being.Full-time employment based in GreeceResponsibilities:Advise clients project teams sites regulatory agencies and thir

PSI Medical Monitors provide medical input to global clinical studies and advise the teams and business partners while always focusing on patients safety and well-being.Full-time employment based in GreeceResponsibilities:Advise clients project teams sites regulatory agencies and thir

PSI Medical Monitors provide medical input to global clinical studies and advise the teams and business partners while always focusing on patients safety and well-being.Full-time office-based in BelgradeResponsibilities:Advise clients project teams sites regulatory agencies and third-

PSI Medical Monitors provide medical input to global clinical studies and advise the teams and business partners while always focusing on patients safety and well-being.Full-time office-based in BelgradeResponsibilities:Advise clients project teams sites regulatory agencies and third-

PSI Medical Monitors provide medical input to global clinical studies and advise the teams and business partners while always focusing on patients safety and well-being.Full-time office-based in Banja LukaResponsibilities:Advise clients project teams sites regulatory agencies and thir

PSI Medical Monitors provide medical input to global clinical studies and advise the teams and business partners while always focusing on patients safety and well-being.Full-time office-based in Banja LukaResponsibilities:Advise clients project teams sites regulatory agencies and thir

PSI Medical Monitors provide medical input to global clinical studies and advise the teams and business partners while always focusing on patients safety and well-being.Responsibilities:Advise clients project teams sites regulatory agencies and third-party vendors on medical mattersCo

PSI Medical Monitors provide medical input to global clinical studies and advise the teams and business partners while always focusing on patients safety and well-being.Responsibilities:Advise clients project teams sites regulatory agencies and third-party vendors on medical mattersCo

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

PSI Medical Monitors provide medical input to global clinical studies and advise the teams and business partners while always focusing on patients safety and well-being.Full-time employment based in EstoniaResponsibilities:Advise clients project teams sites regulatory agencies and thi

PSI Medical Monitors provide medical input to global clinical studies and advise the teams and business partners while always focusing on patients safety and well-being.Full-time employment based in EstoniaResponsibilities:Advise clients project teams sites regulatory agencies and thi

PSI Medical Monitors provide medical input to global clinical studies and advise the teams and business partners while always focusing on patients safety and well-being.Full-time employment based in Sofia BulgariaResponsibilities:Advise clients project teams sites regulatory agencies

PSI Medical Monitors provide medical input to global clinical studies and advise the teams and business partners while always focusing on patients safety and well-being.Full-time employment based in Sofia BulgariaResponsibilities:Advise clients project teams sites regulatory agencies

PSI Medical Monitors provide medical input to global clinical studies and advise the teams and business partners while always focusing on patients safety and well-being.Full-time employment based in Zagreb CroatiaResponsibilities:Advise clients project teams sites regulatory agencies

PSI Medical Monitors provide medical input to global clinical studies and advise the teams and business partners while always focusing on patients safety and well-being.Full-time employment based in Zagreb CroatiaResponsibilities:Advise clients project teams sites regulatory agencies

PSI Medical Monitors provide medical input to global clinical studies and advise the teams and business partners while always focusing on patients safety and well-being.Full-time home-based employment in LatviaResponsibilities:Advise clients project teams sites regulatory agencies and

PSI Medical Monitors provide medical input to global clinical studies and advise the teams and business partners while always focusing on patients safety and well-being.Full-time home-based employment in LatviaResponsibilities:Advise clients project teams sites regulatory agencies and

PSI Medical Monitors provide medical input to global clinical studies and advise the teams and business partners while always focusing on patients safety and well-being.Full-time employment based in Czech RepublicResponsibilities:Advise clients project teams sites regulatory agencies

PSI Medical Monitors provide medical input to global clinical studies and advise the teams and business partners while always focusing on patients safety and well-being.Full-time employment based in Czech RepublicResponsibilities:Advise clients project teams sites regulatory agencies

PSI Medical Monitors provide medical input to global clinical studies and advise the teams and business partners while always focusing on patients safety and well-being.Full-time employment based in FranceResponsibilities:Advise clients project teams sites regulatory agencies and thir

PSI Medical Monitors provide medical input to global clinical studies and advise the teams and business partners while always focusing on patients safety and well-being.Full-time employment based in FranceResponsibilities:Advise clients project teams sites regulatory agencies and thir

PSI Medical Monitors provide medical input to global clinical studies and advise the teams and business partners while always focusing on patients safety and well-being.Full-time employment in RomaniaResponsibilities:Advise clients project teams sites regulatory agencies and third-par

PSI Medical Monitors provide medical input to global clinical studies and advise the teams and business partners while always focusing on patients safety and well-being.Full-time employment in RomaniaResponsibilities:Advise clients project teams sites regulatory agencies and third-par