PSI CRO

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 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

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 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

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

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

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

We 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 for troubleshooting and diagnosing desktop co

We 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 for troubleshooting and diagnosing desktop co

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

Clincial Data Manager plays a critical role in the clinical research project. If you are detail-oriented and committed to quality able to work with large volume of clinical or medical data you might be the professional we are looking for.Please submit your CV in EnglishResponsibilitie

Clincial Data Manager plays a critical role in the clinical research project. If you are detail-oriented and committed to quality able to work with large volume of clinical or medical data you might be the professional we are looking for.Please submit your CV in EnglishResponsibilitie

In this role you will be responsible for building maintaining and optimizing infrastructure CI/CD pipelines and deployment processes across multiple environments.Full-time permanent employment in KazakhstanKey ResponsibilitiesTroubleshoot system issues using logs diagnostics and monit

In this role you will be responsible for building maintaining and optimizing infrastructure CI/CD pipelines and deployment processes across multiple environments.Full-time permanent employment in KazakhstanKey ResponsibilitiesTroubleshoot system issues using logs diagnostics and monit

In this role you will be responsible for building maintaining and optimizing infrastructure CI/CD pipelines and deployment processes across multiple environments.Key ResponsibilitiesTroubleshoot system issues using logs diagnostics and monitoring toolsDevelop and maintain automation s

In this role you will be responsible for building maintaining and optimizing infrastructure CI/CD pipelines and deployment processes across multiple environments.Key ResponsibilitiesTroubleshoot system issues using logs diagnostics and monitoring toolsDevelop and maintain automation s

In this role you will be responsible for building maintaining and optimizing infrastructure CI/CD pipelines and deployment processes across multiple environments.Full-time permanent employment in EstoniaKey Responsibilities:Troubleshoot system issues using logs diagnostics and monitor

In this role you will be responsible for building maintaining and optimizing infrastructure CI/CD pipelines and deployment processes across multiple environments.Full-time permanent employment in EstoniaKey Responsibilities:Troubleshoot system issues using logs diagnostics and monitor

Please submit your CV in English.Be the point of contact with customs authorities courier companies and carriers for different issues and negotiationStay abreast of changes in import or export laws/regulationsClassify goods according to the tariff coding systemManage track maintain an

Please submit your CV in English.Be the point of contact with customs authorities courier companies and carriers for different issues and negotiationStay abreast of changes in import or export laws/regulationsClassify goods according to the tariff coding systemManage track maintain an

As a CRA 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 and investigators.  Your

As a CRA 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 and investigators.  Your

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

Please provide your CV in English.The scope of responsibilities will include:Constantly maintain and generate relations with Investigative Sites;Maintain and refine the internal site database in cooperation with Study Startup Clinical Operations and Process Improvement;Participate in

Please provide your CV in English.The scope of responsibilities will include:Constantly maintain and generate relations with Investigative Sites;Maintain and refine the internal site database in cooperation with Study Startup Clinical Operations and Process Improvement;Participate in