دوام كامل

Manage deliver and/or perform full clinical site monitoring services for one or more projects which may include multiple services be complex in nature and/or run on a multinational -house based position responsible for the design and oversight of project monitoring services including

Manage deliver and/or perform full clinical site monitoring services for one or more projects which may include multiple services be complex in nature and/or run on a multinational -house based position responsible for the design and oversight of project monitoring services including

قدم الآن

Alimentiv

دوام كامل

In this role you will lead medical writing projects for Clinical Research Scientists Academic partners Sponsors and/or the Corporation. Interpret and translate complex technical research methodologies data or messaging into clinical development plans and regulatory documents (protocol

In this role you will lead medical writing projects for Clinical Research Scientists Academic partners Sponsors and/or the Corporation. Interpret and translate complex technical research methodologies data or messaging into clinical development plans and regulatory documents (protocol

قدم الآن
دوام كامل

Manage deliver and/or perform full clinical site monitoring services for one or more projects which may include multiple services be complex in nature and/or run on a multinational -house based position responsible for the design and oversight of project monitoring services including

Manage deliver and/or perform full clinical site monitoring services for one or more projects which may include multiple services be complex in nature and/or run on a multinational -house based position responsible for the design and oversight of project monitoring services including

قدم الآن

Alimentiv

دوام كامل

In this role you will be providing unbiased medical guidance to clinical sites and internal and external study operations teams. You will also be providing therapeutic and compound training medical guidance on protocol compliance ensuring medical congruency at subject and study level

In this role you will be providing unbiased medical guidance to clinical sites and internal and external study operations teams. You will also be providing therapeutic and compound training medical guidance on protocol compliance ensuring medical congruency at subject and study level

قدم الآن

Alimentiv

دوام كامل

In this role you will be providing unbiased medical guidance to clinical sites and internal and external study operations teams. You will also be providing therapeutic and compound training medical guidance on protocol compliance ensuring medical congruency at subject and study level

In this role you will be providing unbiased medical guidance to clinical sites and internal and external study operations teams. You will also be providing therapeutic and compound training medical guidance on protocol compliance ensuring medical congruency at subject and study level

قدم الآن

Alimentiv

دوام كامل

In this role you will be providing unbiased medical guidance to clinical sites and internal and external study operations teams. You will also be providing therapeutic and compound training medical guidance on protocol compliance ensuring medical congruency at subject and study level

In this role you will be providing unbiased medical guidance to clinical sites and internal and external study operations teams. You will also be providing therapeutic and compound training medical guidance on protocol compliance ensuring medical congruency at subject and study level

قدم الآن

Acts as the primary regional representative for the execution and delivery of clinical project(s); cultivate excellent Sponsor relationships provide project oversight assisting with project delivery services as required ensuring that projects are adequately and appropriately staffed m

Acts as the primary regional representative for the execution and delivery of clinical project(s); cultivate excellent Sponsor relationships provide project oversight assisting with project delivery services as required ensuring that projects are adequately and appropriately staffed m

قدم الآن

Alimentiv

دوام كامل

In this role you will be providing unbiased medical guidance to clinical sites and internal and external study operations teams. You will also be providing therapeutic and compound training medical guidance on protocol compliance ensuring medical congruency at subject and study level

In this role you will be providing unbiased medical guidance to clinical sites and internal and external study operations teams. You will also be providing therapeutic and compound training medical guidance on protocol compliance ensuring medical congruency at subject and study level

قدم الآن
دوام كامل

Responsible for the clinical operations of a project within a defined regional/global level. Provides oversight of project deliverables assigned Clinical Research Associate (CRAs) and Investigator sites in accordance with the Monitoring Plan Protocol Good Clinical Practice (GCP) ICH g

Responsible for the clinical operations of a project within a defined regional/global level. Provides oversight of project deliverables assigned Clinical Research Associate (CRAs) and Investigator sites in accordance with the Monitoring Plan Protocol Good Clinical Practice (GCP) ICH g

قدم الآن

Dont see an opening that quite matches what youre looking for or not ready to make a move yet Let us know!We are proactively inviting qualified candidates to join our talent pool for anticipated Clinical Research Associate needs (across multiple seniority levels) to support our Clinic

Dont see an opening that quite matches what youre looking for or not ready to make a move yet Let us know!We are proactively inviting qualified candidates to join our talent pool for anticipated Clinical Research Associate needs (across multiple seniority levels) to support our Clinic

قدم الآن
دوام كامل

Responsible for the clinical operations of a project within a defined regional/global level. Provides oversight of project deliverables assigned Clinical Research Associate (CRAs) and Investigator sites in accordance with the Monitoring Plan Protocol Good Clinical Practice (GCP) ICH g

Responsible for the clinical operations of a project within a defined regional/global level. Provides oversight of project deliverables assigned Clinical Research Associate (CRAs) and Investigator sites in accordance with the Monitoring Plan Protocol Good Clinical Practice (GCP) ICH g

قدم الآن
دوام كامل

Responsible for the clinical operations of a project within a defined regional/global level. Provides oversight of project deliverables assigned Clinical Research Associate (CRAs) and Investigator sites in accordance with the Monitoring Plan Protocol Good Clinical Practice (GCP) ICH g

Responsible for the clinical operations of a project within a defined regional/global level. Provides oversight of project deliverables assigned Clinical Research Associate (CRAs) and Investigator sites in accordance with the Monitoring Plan Protocol Good Clinical Practice (GCP) ICH g

قدم الآن

The Manager Software Development & Testing is a hands-on people leader responsible for the day-to-day execution quality and delivery of software solutions within Alimentivs clinical imaging ecosystem. This role combines technical leadership with team management to ensure software is b

The Manager Software Development & Testing is a hands-on people leader responsible for the day-to-day execution quality and delivery of software solutions within Alimentivs clinical imaging ecosystem. This role combines technical leadership with team management to ensure software is b

قدم الآن
دوام كامل

Responsible for processing monitoring maintaining and reporting of corporate and project-related accounts payable accounts receivable credit and collections expense report processing project payments and/or related financial transactions on a timely basis in accordance with project co

Responsible for processing monitoring maintaining and reporting of corporate and project-related accounts payable accounts receivable credit and collections expense report processing project payments and/or related financial transactions on a timely basis in accordance with project co

قدم الآن
دوام كامل

Responsible for providing senior support in planning organizing and/or evaluating the day-to-day delivery of global quality assurance (QA) services. Responsible for supporting the business in quality assurance policy planning and development ongoing quality improvement through clinica

Responsible for providing senior support in planning organizing and/or evaluating the day-to-day delivery of global quality assurance (QA) services. Responsible for supporting the business in quality assurance policy planning and development ongoing quality improvement through clinica

قدم الآن
دوام كامل

Manage deliver and/or perform full clinical site monitoring services for one or more projects which may include multiple services be complex in nature and/or run on a multinational -house based position responsible for the design and oversight of project monitoring services including

Manage deliver and/or perform full clinical site monitoring services for one or more projects which may include multiple services be complex in nature and/or run on a multinational -house based position responsible for the design and oversight of project monitoring services including

قدم الآن
دوام كامل

Manage deliver and/or perform full clinical site monitoring services for one or more projects which may include multiple services be complex in nature and/or run on a multinational -house based position responsible for the design and oversight of project monitoring services including

Manage deliver and/or perform full clinical site monitoring services for one or more projects which may include multiple services be complex in nature and/or run on a multinational -house based position responsible for the design and oversight of project monitoring services including

قدم الآن
دوام كامل

Job Title:Production & Assembly CoordinatorJob Location:Amsterdam NL (on-site)Job Salary: 31000 - 35000 EUREmployment Type:Full time Limited TermJob Reports To:Manager LogisticsDepartment/Unit Name: Clinical Operations - LogisticsJob Summary: Responsible for assembly testing and decom

Job Title:Production & Assembly CoordinatorJob Location:Amsterdam NL (on-site)Job Salary: 31000 - 35000 EUREmployment Type:Full time Limited TermJob Reports To:Manager LogisticsDepartment/Unit Name: Clinical Operations - LogisticsJob Summary: Responsible for assembly testing and decom

قدم الآن