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

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

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.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.Home-Based or office based/hybrid in Madrid or BarcelonaResponsibilities:Advise clients project teams sites regulato

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.Home-Based or office based/hybrid in Madrid or BarcelonaResponsibilities:Advise clients project teams sites regulato

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-

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.Home-Based in Italy or office based/hybrid in MilanResponsibilities:Advise clients project teams sites regulatory ag

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.Home-Based in Italy or office based/hybrid in MilanResponsibilities:Advise clients project teams sites regulatory ag

Acts as primary communication point for project teams and company departments regarding clinical data management.Acts as primary communication point for clients/vendors for all data management aspects of clinical projects and clinical data management reporting.Responsible for the supe

Acts as primary communication point for project teams and company departments regarding clinical data management.Acts as primary communication point for clients/vendors for all data management aspects of clinical projects and clinical data management reporting.Responsible for the supe

Acts as primary communication point for project teams and company departments regarding clinical data management.Acts as primary communication point for clients/vendors for all data management aspects of clinical projects and clinical data management reporting.Responsible for the supe

Acts as primary communication point for project teams and company departments regarding clinical data management.Acts as primary communication point for clients/vendors for all data management aspects of clinical projects and clinical data management reporting.Responsible for the supe

Business Development Representative 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 Developm

Business Development Representative 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 Developm

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 employment in SpainYou wil

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 employment in SpainYou wil

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

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

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

Writes edits and reviews documents including informed consent forms patient information and other project-specific clinical documentation.Writes edits reviews finalizes and tracks clinical study report (CSR) patient safety narratives.Collects and tracks documents for CSR appendices in

Writes edits and reviews documents including informed consent forms patient information and other project-specific clinical documentation.Writes edits reviews finalizes and tracks clinical study report (CSR) patient safety narratives.Collects and tracks documents for CSR appendices in