PSI CRO

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

We are looking for professional qualified and enthusiastic candidates to take up a full-time position of a Junior IT Systems Administrator to provide daily technical support.The scope of responsibilities will include:Supervised responsibility for troubleshooting and diagnosing desktop

We are looking for professional qualified and enthusiastic candidates to take up a full-time position of a Junior IT Systems Administrator to provide daily technical support.The scope of responsibilities will include:Supervised responsibility for troubleshooting and diagnosing desktop

Take your career to the next level and be involved in leading the study startup processes in Japan. You will provide direct operational support to project teams from project start until activation and ensure that PSI clinical projects start smoothly and on time.  Hybrid workstyle (Tok

Take your career to the next level and be involved in leading the study startup processes in Japan. You will provide direct operational support to project teams from project start until activation and ensure that PSI clinical projects start smoothly and on time.  Hybrid workstyle (Tok

As a Senior CRA I you will work on the frontline of communication with project stakeholders ensuring timelines targets. You will have the opportunity to work on clinical studies in various therapeutic areas and indications while maintaining the highest quality standards in the industr

As a Senior CRA I you will work on the frontline of communication with project stakeholders ensuring timelines targets. You will have the opportunity to work on clinical studies in various therapeutic areas and indications while maintaining the highest quality standards in the industr

Acts as a communication line for project teams regarding clinical data managementMaintains TMF/eTMFTrains Assistant Data ManagerIs involved in clinical data management activities including but not limited to:Supporting development of study documentation (eCRF Requirements Edit Checks

Acts as a communication line for project teams regarding clinical data managementMaintains TMF/eTMFTrains Assistant Data ManagerIs involved in clinical data management activities including but not limited to:Supporting development of study documentation (eCRF Requirements Edit Checks

The Lead Data Manager will be responsible for all data management activities in large complex studies under general supervision or working under minimal supervision on data management activities for small to medium sized projects.  CommunicationPrimary communication point for project

The Lead Data Manager will be responsible for all data management activities in large complex studies under general supervision or working under minimal supervision on data management activities for small to medium sized projects.  CommunicationPrimary communication point for project

The Manager Business Development is a pivotal role responsible for active promotion of Milestone One brand acquiring new clinics building a site network of Milestone One and managing Clinical Trials from vendor selection through site contracting. The Manager Business Development colla

The Manager Business Development is a pivotal role responsible for active promotion of Milestone One brand acquiring new clinics building a site network of Milestone One and managing Clinical Trials from vendor selection through site contracting. The Manager Business Development colla

As part of PSIs Medical Monitoring team you will join our international group of medical professionals build a career on the frontline of medical science and use your knowledge and expertise to help bring new medications to patients that need them.Full-time employment Office location:

As part of PSIs Medical Monitoring team you will join our international group of medical professionals build a career on the frontline of medical science and use your knowledge and expertise to help bring new medications to patients that need them.Full-time employment Office location:

As part of PSIs Medical Monitoring team you will join our international group of medical professionals build a career on the frontline of medical science and use your knowledge and expertise to help bring new medications to patients that need them.Full-time employment based in Bangkok

As part of PSIs Medical Monitoring team you will join our international group of medical professionals build a career on the frontline of medical science and use your knowledge and expertise to help bring new medications to patients that need them.Full-time employment based in Bangkok

Join our international team and be the key support to clinical research projects streamlining communication maintaining systems and managing documents & information. You will focus on facilitating research projects of novel medicinal products while taking a step further in your profes

Join our international team and be the key support to clinical research projects streamlining communication maintaining systems and managing documents & information. You will focus on facilitating research projects of novel medicinal products while taking a step further in your profes

As part of PSIs Medical Monitoring team you will join our international group of medical professionals build a career on the frontline of medical science and use your knowledge and expertise to help bring new medications to patients that need them.Full-time employment based in SeoulRe

As part of PSIs Medical Monitoring team you will join our international group of medical professionals build a career on the frontline of medical science and use your knowledge and expertise to help bring new medications to patients that need them.Full-time employment based in SeoulRe

As part of PSIs Medical Monitoring team you will join our international group of medical professionals build a career on the frontline of medical science and use your knowledge and expertise to help bring new medications to patients that need them.Full-time employment based in Austral

As part of PSIs Medical Monitoring team you will join our international group of medical professionals build a career on the frontline of medical science and use your knowledge and expertise to help bring new medications to patients that need them.Full-time employment based in Austral

s part of PSIs Medical Monitoring team you will join our international group of medical professionals build a career on the frontline of medical science and use your knowledge and expertise to help bring new medications to patients that need them.Full-time employment based in Singapor

s part of PSIs Medical Monitoring team you will join our international group of medical professionals build a career on the frontline of medical science and use your knowledge and expertise to help bring new medications to patients that need them.Full-time employment based in Singapor

As part of PSIs Medical Monitoring team you will join our international group of medical professionals build a career on the frontline of medical science and use your knowledge and expertise to help bring new medications to patients that need them.Full-time employment based in TaipeiR

As part of PSIs Medical Monitoring team you will join our international group of medical professionals build a career on the frontline of medical science and use your knowledge and expertise to help bring new medications to patients that need them.Full-time employment based in TaipeiR

We are currently looking for a knowledgeable and proactive SAS Developer to join our global Data Management team.Please note the official PSI CRO job title will be: Senior Database Developer.If you are keen to provide the full range of clinical database development and programming ser

We are currently looking for a knowledgeable and proactive SAS Developer to join our global Data Management team.Please note the official PSI CRO job title will be: Senior Database Developer.If you are keen to provide the full range of clinical database development and programming ser

We are currently looking for a knowledgeable and proactive SAS Developer to join our global Data Management team.Please note the official PSI CRO job title will be: Senior Database Developer.If you are keen to provide the full range of clinical database development and programming ser

We are currently looking for a knowledgeable and proactive SAS Developer to join our global Data Management team.Please note the official PSI CRO job title will be: Senior Database Developer.If you are keen to provide the full range of clinical database development and programming ser

The Project Coordination Associate supervises and coordinates trial administrative support management of trial records site management and communication with the investigator sites the sponsor trial vendors and members of the project team. This function operates at a regional or globa

The Project Coordination Associate supervises and coordinates trial administrative support management of trial records site management and communication with the investigator sites the sponsor trial vendors and members of the project team. This function operates at a regional or globa

The Project Coordination Associate supervises and coordinates trial administrative support management of trial records site management and communication with the investigator sites the sponsor trial vendors and members of the project team. This function operates at a regional or globa

The Project Coordination Associate supervises and coordinates trial administrative support management of trial records site management and communication with the investigator sites the sponsor trial vendors and members of the project team. This function operates at a regional or globa

We are seeking a detail-oriented and analytical Medical Reviewer to join our team in this role you will be responsible for reviewing and evaluating medical content ensuring accuracy consistency and compliance with regulatory standards.Conduct medical review of clinical database: perf

We are seeking a detail-oriented and analytical Medical Reviewer to join our team in this role you will be responsible for reviewing and evaluating medical content ensuring accuracy consistency and compliance with regulatory standards.Conduct medical review of clinical database: perf

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