PSI CRO

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

ResponsibilitiesCoordinating the preparation of contracts for employees and contractors.Ensuring that draft contracts reflect the agreed terms (role scope compensation benefits) and basic local requirements before submission for approval and signature.Monitoring the full contract life

ResponsibilitiesCoordinating the preparation of contracts for employees and contractors.Ensuring that draft contracts reflect the agreed terms (role scope compensation benefits) and basic local requirements before submission for approval and signature.Monitoring the full contract life

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. Yo

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. Yo

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: Maintains study-specific and corporate startup tracking systems.Facilitates site

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: Maintains study-specific and corporate startup tracking systems.Facilitates site

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

We are seeking a highly motivated Lead Software Developer (AI) to lead the architecture development and implementation of AI-driven solutions supporting Data Management processes within a Clinical Research Organization (CRO). This role is ideal for a professional who can independently

We are seeking a highly motivated Lead Software Developer (AI) to lead the architecture development and implementation of AI-driven solutions supporting Data Management processes within a Clinical Research Organization (CRO). This role is ideal for a professional who can independently

1. Core responsibilities:1.1. Provides administrative support to the Study Startup department with processes critical for site activation.1.2. Supports Feasibility department with feasibility research and site identification activities.1.3. Maintains project-specific tracking systems

1. Core responsibilities:1.1. Provides administrative support to the Study Startup department with processes critical for site activation.1.2. Supports Feasibility department with feasibility research and site identification activities.1.3. Maintains project-specific tracking systems

SCOPE OF RESPONSIBILITIES1. Core responsibilities (the scope of responsibilities may vary and is dependent on project allocations and study startup process specifics in the country/region)1.1. The Study Startup Manager leads study startup in 1 to 3 assigned countries on projects withi

SCOPE OF RESPONSIBILITIES1. Core responsibilities (the scope of responsibilities may vary and is dependent on project allocations and study startup process specifics in the country/region)1.1. The Study Startup Manager leads study startup in 1 to 3 assigned countries on projects withi

Take your career to the next level and lead challenging full-service global clinical research projects managing the full scope of responsibilities and getting hands-on involvement in every aspect of the study.Your responsibilities will include: (Tokyo or Osaka office)Management of cou

Take your career to the next level and lead challenging full-service global clinical research projects managing the full scope of responsibilities and getting hands-on involvement in every aspect of the study.Your responsibilities will include: (Tokyo or Osaka office)Management of cou