PSI CRO

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

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

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

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.This is an office-based position from our Bangalore office.You will: Collaborate with the pr

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.This is an office-based position from our Bangalore office.You will: Collaborate with the pr

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

Are you an experienced Clinical Research Associate (CRA) looking for new development opportunities This might be a great opportunity for you!We have an exciting opening for a Referral Network Specialist which is a dynamic role designed to take your career to the next level. Use your e

Are you an experienced Clinical Research Associate (CRA) looking for new development opportunities This might be a great opportunity for you!We have an exciting opening for a Referral Network Specialist which is a dynamic role designed to take your career to the next level. Use your e

Were searching for a knowledgeable team-oriented CRA II to manage the clinical aspects of full-service global projects in Japan. As a CRA II at PSI you will work on the frontline of communication with project stakeholders ensuring timelines targets and standards of clinical research p

Were searching for a knowledgeable team-oriented CRA II to manage the clinical aspects of full-service global projects in Japan. As a CRA II at PSI you will work on the frontline of communication with project stakeholders ensuring timelines targets and standards of clinical research p

Join our international team as a Coordinator Regional F&A where you will play a key role in ensuring accurate and timely out-of-pocket (OOP) expense reporting across the region. You will be able to take ownership of financial processes collaborate with cross-functional teams and contr

Join our international team as a Coordinator Regional F&A where you will play a key role in ensuring accurate and timely out-of-pocket (OOP) expense reporting across the region. You will be able to take ownership of financial processes collaborate with cross-functional teams and contr

SCOPE OF RESPONSIBILITIES1. Lead Monitoring1.1. Supports investigator/ site feasibility and identification process1.2. Monitors trial timelines and trial participant enrollment implements respective corrective and preventive measures1.3. Reviews monitoring visit reports for all visit

SCOPE OF RESPONSIBILITIES1. Lead Monitoring1.1. Supports investigator/ site feasibility and identification process1.2. Monitors trial timelines and trial participant enrollment implements respective corrective and preventive measures1.3. Reviews monitoring visit reports for all visit

In this role you will streamline activities of project teams in Japan and ensure consistency of Clinical Operations processes across regions. You will ensure meeting study milestones by project teams on a country level report study progress to clients and global stakeholders.The scope

In this role you will streamline activities of project teams in Japan and ensure consistency of Clinical Operations processes across regions. You will ensure meeting study milestones by project teams on a country level report study progress to clients and global stakeholders.The scope

This is a hybrid role with 2 days in the Japan (Tokyo or Osaka) office and 3 days working from homeFull-Cycle AccountingProcess all daily accounting transactions including vendor invoices payments bank entries journal postings and intercompany transactions.Maintain accurate records ac

This is a hybrid role with 2 days in the Japan (Tokyo or Osaka) office and 3 days working from homeFull-Cycle AccountingProcess all daily accounting transactions including vendor invoices payments bank entries journal postings and intercompany transactions.Maintain accurate records ac

This role is responsible for leading and supporting architectural fit-out and construction-related projects across PSIs office portfolio with primary focus on the USA and Canada regions. The position combines architectural planning project management contractor coordination and real e

This role is responsible for leading and supporting architectural fit-out and construction-related projects across PSIs office portfolio with primary focus on the USA and Canada regions. The position combines architectural planning project management contractor coordination and real e

This is a hybrid role with 2 days in the Oxfordshire office and 3 days working from homeFull-Cycle AccountingProcess all daily accounting transactions including vendor invoices payments bank entries journal postings and intercompany transactions.Maintain accurate records across genera

This is a hybrid role with 2 days in the Oxfordshire office and 3 days working from homeFull-Cycle AccountingProcess all daily accounting transactions including vendor invoices payments bank entries journal postings and intercompany transactions.Maintain accurate records across genera