Alimentiv

Positions available: 1 (remote based Canada)Must be fluent in English and FrenchManage 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 re

Positions available: 1 (remote based Canada)Must be fluent in English and FrenchManage 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 re

The AI Enablement Specialist supports the adoption of artificial intelligence tools across Alimentiv by providing structured training practical guidance and implementation support to staff at all levels. This role serves as the primary liaison between technology teams and end users tr

The AI Enablement Specialist supports the adoption of artificial intelligence tools across Alimentiv by providing structured training practical guidance and implementation support to staff at all levels. This role serves as the primary liaison between technology teams and end users tr

As a member of the Medical Writing team the Grant writer will work collaboratively with internal stakeholders and team members identify submit and follow up on funding opportunities for research conducted or facilitated by the medical R&D group.Identify Funding Opportunities Systemati

As a member of the Medical Writing team the Grant writer will work collaboratively with internal stakeholders and team members identify submit and follow up on funding opportunities for research conducted or facilitated by the medical R&D group.Identify Funding Opportunities Systemati

Provide administrative clerical implementation and/or processing support to the project teams and stakeholders. Assist with document/process/report development testing tracking distribution and management. Coordinate meetings presentations and training activities facilitate billing an

Provide administrative clerical implementation and/or processing support to the project teams and stakeholders. Assist with document/process/report development testing tracking distribution and management. Coordinate meetings presentations and training activities facilitate billing an

In this role you will be responsible for supporting the execution of core IRT (Interactive Response Technology) management activities across assigned clinical projects ensuring alignment with sponsor requirements regulatory standards and industry best practices. Collaborates cross-fun

In this role you will be responsible for supporting the execution of core IRT (Interactive Response Technology) management activities across assigned clinical projects ensuring alignment with sponsor requirements regulatory standards and industry best practices. Collaborates cross-fun

Support Project Management Regulatory and Contract and Legal in all site-related start-up activities. Establish relationships with study personnel at sites and act as main Alimentiv contact during site start-up. Prepare distribute and follow-up on start-up documents with sites. Plan a

Support Project Management Regulatory and Contract and Legal in all site-related start-up activities. Establish relationships with study personnel at sites and act as main Alimentiv contact during site start-up. Prepare distribute and follow-up on start-up documents with sites. Plan a

ABOUT ALIMENTIVAlimentiv is a global CRO with a singular focus: advancing therapies for patients with gastrointestinal diseases. GI is our WHY and for more than 30 years that purpose has driven our scientific rigour operational excellence and deep therapeutic expertise including suppo

ABOUT ALIMENTIVAlimentiv is a global CRO with a singular focus: advancing therapies for patients with gastrointestinal diseases. GI is our WHY and for more than 30 years that purpose has driven our scientific rigour operational excellence and deep therapeutic expertise including suppo

ABOUT ALIMENTIVAlimentiv is a global CRO with a singular focus: advancing therapies for patients with gastrointestinal diseases. GI is our WHY and for more than 30 years that purpose has driven our scientific rigour operational excellence and deep therapeutic expertise including suppo

ABOUT ALIMENTIVAlimentiv is a global CRO with a singular focus: advancing therapies for patients with gastrointestinal diseases. GI is our WHY and for more than 30 years that purpose has driven our scientific rigour operational excellence and deep therapeutic expertise including suppo

In this role you will be responsible for supporting the execution of core IRT (Interactive Response Technology) management activities across assigned clinical projects ensuring alignment with sponsor requirements regulatory standards and industry best practices. Collaborates cross-fun

In this role you will be responsible for supporting the execution of core IRT (Interactive Response Technology) management activities across assigned clinical projects ensuring alignment with sponsor requirements regulatory standards and industry best practices. Collaborates cross-fun

This position will support and observe clinical site monitoring services inhouse and provide monitoring and site management activities for full-service studies assessing for protocol SOP and regulatory compliance. Responsibilities include site management activities to help drive inves

This position will support and observe clinical site monitoring services inhouse and provide monitoring and site management activities for full-service studies assessing for protocol SOP and regulatory compliance. Responsibilities include site management activities to help drive inves

In this role you will be providing medical writing services and consultation to Clinical Research Scientists Academic partners Sponsors and/or the Corporation which may include researching writing reviewing and editing scientific information coordinating document reviews with authors

In this role you will be providing medical writing services and consultation to Clinical Research Scientists Academic partners Sponsors and/or the Corporation which may include researching writing reviewing and editing scientific information coordinating document reviews with authors

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

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

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

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

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

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

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

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

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