Alimentiv

The Software Project Manager will drive the successful execution and delivery of software projects within the Medical Imaging product line. This role is primarily responsible for managing all stages of project planning execution and delivery ensuring alignment with our organizations s

The Software Project Manager will drive the successful execution and delivery of software projects within the Medical Imaging product line. This role is primarily responsible for managing all stages of project planning execution and delivery ensuring alignment with our organizations s

Responsible for providing global administrative support in the areas of employee experiencetraining employee on and off-boarding payroll benefits and human resource (HR) recordsmaintenance (paper and electronic).ResponsibilitiesTriage and respond to employee inquiriesProcess track mai

Responsible for providing global administrative support in the areas of employee experiencetraining employee on and off-boarding payroll benefits and human resource (HR) recordsmaintenance (paper and electronic).ResponsibilitiesTriage and respond to employee inquiriesProcess track mai

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

This is an exciting opportunity to join a new state-of the-art CLIA laboratory focused on accelerating biomarker and drug development. You will have the opportunity to use your entrepreneurial spirit and apply your knowledge/experience to operationalize the plan for the new laboratory

This is an exciting opportunity to join a new state-of the-art CLIA laboratory focused on accelerating biomarker and drug development. You will have the opportunity to use your entrepreneurial spirit and apply your knowledge/experience to operationalize the plan for the new laboratory

Location:London OntarioJob Salary:$42000 - $70000Job Title:Image Service Coordinator (Full-time permanent)Department:Image ServicesNote: This opening is for the overnight shift with a shift window of 11:00 PM 8:00 AM EST.Job Summary:Assist in the execution of all Image Services activ

Location:London OntarioJob Salary:$42000 - $70000Job Title:Image Service Coordinator (Full-time permanent)Department:Image ServicesNote: This opening is for the overnight shift with a shift window of 11:00 PM 8:00 AM EST.Job Summary:Assist in the execution of all Image Services activ

The Imaging Research and Development Associate will assist with providing the Clinical Project Management Data Management and Medical Leadership teams with medical scientific and operational advice/support for Central Image Management Solution (CIMS) clinical trials. Act as a point of

The Imaging Research and Development Associate will assist with providing the Clinical Project Management Data Management and Medical Leadership teams with medical scientific and operational advice/support for Central Image Management Solution (CIMS) clinical trials. Act as a point of

Responsible for the application of biostatistical methods to support clinical trials and data management including statistical planning design analysis and reporting throughout the project life cycle in accordance with project organizational and regulatory standards. Act as subject ma

Responsible for the application of biostatistical methods to support clinical trials and data management including statistical planning design analysis and reporting throughout the project life cycle in accordance with project organizational and regulatory standards. Act as subject ma

Responsible for the application of biostatistical methods to support clinical trials and data management including statistical planning design analysis and reporting throughout the project life cycle in accordance with project organizational and regulatory standards. Act as subject ma

Responsible for the application of biostatistical methods to support clinical trials and data management including statistical planning design analysis and reporting throughout the project life cycle in accordance with project organizational and regulatory standards. Act as subject ma

Responsible to plan manage organize evaluate and/or report on the day delivery of the Clinical Monitoring unit (Clinical Operations Leads).Role includes policy and process development and improvement product quality site and compliance monitoring staff resource planning and staff and

Responsible to plan manage organize evaluate and/or report on the day delivery of the Clinical Monitoring unit (Clinical Operations Leads).Role includes policy and process development and improvement product quality site and compliance monitoring staff resource planning and staff and

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

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

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

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 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

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