PSI CRO

 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 complia

 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 complia

As a Full stack Developer you will be involved in development of projects for internal clients and will provide quality coding to support PSI business processes and operations. You will work on desktop WinForm/Blazor hybrid applications contributing to both new development and ongoing

As a Full stack Developer you will be involved in development of projects for internal clients and will provide quality coding to support PSI business processes and operations. You will work on desktop WinForm/Blazor hybrid applications contributing to both new development and ongoing

As a Full stack Developer you will be involved in development of projects for internal clients and will provide quality coding to support PSI business processes and operations. You will work on desktop WinForms/Blazor hybrid applications contributing to both new development and ongoin

As a Full stack Developer you will be involved in development of projects for internal clients and will provide quality coding to support PSI business processes and operations. You will work on desktop WinForms/Blazor hybrid applications contributing to both new development and ongoin

RESPONSIBILITIES1.1. Supervised responsibility for troubleshooting and diagnosing desktop computer systems and peripheral equipment problems1.2. Supervised responsibility for IT support operations including but not limited to receiving and tracking user requests assigning priority and

RESPONSIBILITIES1.1. Supervised responsibility for troubleshooting and diagnosing desktop computer systems and peripheral equipment problems1.2. Supervised responsibility for IT support operations including but not limited to receiving and tracking user requests assigning priority and

 1. Therapeutic Oversight1.1. Is involved in indication-specific strategy planning and implementation across the assigned therapeutic area.1.2. Compiles and delivers presentations on lessons learned.1.3. Mentors trains and assists department staff in developed strategies and best prac

 1. Therapeutic Oversight1.1. Is involved in indication-specific strategy planning and implementation across the assigned therapeutic area.1.2. Compiles and delivers presentations on lessons learned.1.3. Mentors trains and assists department staff in developed strategies and best prac

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

The Site/Study Coordinator supports a medical institution in clinical trial-related activities. Protocol-specific tasks will be determined by the Principal Investigator considering all local and federal laws and regulations and upon review of competencies observed and documented by Mi

The Site/Study Coordinator supports a medical institution in clinical trial-related activities. Protocol-specific tasks will be determined by the Principal Investigator considering all local and federal laws and regulations and upon review of competencies observed and documented by Mi

The Regional Project Lead manages and coordinates activities of project teams in designated countries and ensures consistency of Clinical Operations processes across regions. They ensure meeting study milestones are met by the project team on a country and regional level.Ensures plann

The Regional Project Lead manages and coordinates activities of project teams in designated countries and ensures consistency of Clinical Operations processes across regions. They ensure meeting study milestones are met by the project team on a country and regional level.Ensures plann

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 systemsWork with large amount of docume

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 systemsWork with large amount of docume

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 Site/Study Coordinator supports a medical institution in clinical trial-related activities. Protocol-specific tasks will be determined by the Principal Investigator considering all local and federal laws and regulations and upon review of competencies observed and documented by Mi

The Site/Study Coordinator supports a medical institution in clinical trial-related activities. Protocol-specific tasks will be determined by the Principal Investigator considering all local and federal laws and regulations and upon review of competencies observed and documented by Mi

Only CVs in English will be consideredIn this role a Clinical Trial Liaison: Acts as a specialized liaison to assist sites with a protocol-tailored approach to increase efficiency of the patient identification and recruitment process. Assists sites in developing and implementing patie

Only CVs in English will be consideredIn this role a Clinical Trial Liaison: Acts as a specialized liaison to assist sites with a protocol-tailored approach to increase efficiency of the patient identification and recruitment process. Assists sites in developing and implementing patie

As a Senior CRA 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 and investigators. 

As a Senior CRA 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 and investigators. 

This is an office-based position in Durham NCWe are looking for professional qualified and enthusiastic candidates to take up a full-time position of a Jr. IT Systems Administrator to provide daily technical support.The scope of responsibilities will include:Supervised responsibility

This is an office-based position in Durham NCWe are looking for professional qualified and enthusiastic candidates to take up a full-time position of a Jr. IT Systems Administrator to provide daily technical support.The scope of responsibilities will include:Supervised responsibility

Only CVs in English will be consideredIn this role a Clinical Trial Liaison: Acts as a specialized liaison to assist sites with a protocol-tailored approach to increase efficiency of the patient identification and recruitment process. Assists sites in developing and implementing patie

Only CVs in English will be consideredIn this role a Clinical Trial Liaison: Acts as a specialized liaison to assist sites with a protocol-tailored approach to increase efficiency of the patient identification and recruitment process. Assists sites in developing and implementing patie

Join our international team and be the key support to clinical research projects as part of the start-up team working in a dynamic multi-functional environment gaining unique skills from various disciplines relevant to clinical research.You will:Facilitate review and negotiation of cl

Join our international team and be the key support to clinical research projects as part of the start-up team working in a dynamic multi-functional environment gaining unique skills from various disciplines relevant to clinical research.You will:Facilitate review and negotiation of cl

Based in ShanghaiOverall Responsibilities- Maintains and refines the internal site database in cooperation with Study Startup Clinical Operations and Process Improvement.- Participates in development of improvement strategies for the site identification process implementation thereof

Based in ShanghaiOverall Responsibilities- Maintains and refines the internal site database in cooperation with Study Startup Clinical Operations and Process Improvement.- Participates in development of improvement strategies for the site identification process implementation thereof

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

Assesses feasibility of research protocols based on knowledge and experience and in accordance with designated criteria to select the most suitable studies for the clinical site.  Supervises the conduct of clinical trials in accordance with ICH GCP applicable regulations procedures an

Assesses feasibility of research protocols based on knowledge and experience and in accordance with designated criteria to select the most suitable studies for the clinical site.  Supervises the conduct of clinical trials in accordance with ICH GCP applicable regulations procedures an

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: Perform study startup activities and support all processes critical for site acti

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: Perform study startup activities and support all processes critical for site acti