PSI CRO

If you are keen to provide administrative document management support to pharmaceutical research projects and be involved in something new outstanding and challenging this job opportunity is perfect for you!Only CVs in English will be considered.Responsibilities for this role include:

If you are keen to provide administrative document management support to pharmaceutical research projects and be involved in something new outstanding and challenging this job opportunity is perfect for you!Only CVs in English will be considered.Responsibilities for this role include:

What Youll DoBuild our presence in the marketDevelop and execute the country expansion strategy.Represent the company within the local clinical research community.Build relationships with key investigators healthcare institutions sponsors CROs and other industry stakeholders.Identify

What Youll DoBuild our presence in the marketDevelop and execute the country expansion strategy.Represent the company within the local clinical research community.Build relationships with key investigators healthcare institutions sponsors CROs and other industry stakeholders.Identify

What Youll DoBuild our presence in the marketDevelop and execute the country expansion strategy.Represent the company within the local clinical research community.Build relationships with key investigators healthcare institutions sponsors CROs and other industry stakeholders.Identify

What Youll DoBuild our presence in the marketDevelop and execute the country expansion strategy.Represent the company within the local clinical research community.Build relationships with key investigators healthcare institutions sponsors CROs and other industry stakeholders.Identify

As a Senior Clinical Research Associate/ 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

As a Senior Clinical Research Associate/ 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

Join our international team and be the key support to clinical research projects streamlining communication maintaining systems and managing documents & information.Office-based in Munich/PlaneggThe scope of responsibilities will include:Maintenance of databases and tracking systemsWo

Join our international team and be the key support to clinical research projects streamlining communication maintaining systems and managing documents & information.Office-based in Munich/PlaneggThe scope of responsibilities will include:Maintenance of databases and tracking systemsWo

Join our international team and support regulatory aspects of clinical research projects streamlining communication maintaining electronic systems and managing documents.Full-time employment based in Almaty KazakhstanYou will:Be the point of contact for clinical project teams and supp

Join our international team and support regulatory aspects of clinical research projects streamlining communication maintaining electronic systems and managing documents.Full-time employment based in Almaty KazakhstanYou will:Be the point of contact for clinical project teams and supp

Were searching for a knowledgeable team-oriented CRA II to manage the clinical aspects of full-service global projects in Taiwan. 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

Were searching for a knowledgeable team-oriented CRA II to manage the clinical aspects of full-service global projects in Taiwan. 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

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

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

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