Alimentiv

The Alimentiv Site Network Manager will be responsible to drive and deliver on the Alimentiv Site Network (ASN) Strategy. This position will drive the project management process optimization and growth of the ASNglobally through identification outreach collaboration with and onboardin

The Alimentiv Site Network Manager will be responsible to drive and deliver on the Alimentiv Site Network (ASN) Strategy. This position will drive the project management process optimization and growth of the ASNglobally through identification outreach collaboration with and onboardin

The Inside Sales and Marketing Manager generates qualifies and converts high-value commercial opportunities for AcelaBio by combining targeted inside sales execution with integrated marketing program delivery. Reporting to the Vice President Business Development this role serves as th

The Inside Sales and Marketing Manager generates qualifies and converts high-value commercial opportunities for AcelaBio by combining targeted inside sales execution with integrated marketing program delivery. Reporting to the Vice President Business Development this role serves as th

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

Responsible for the day-to-day activities and delivery of Global Regulatory Affairs support services. Role will include management of clinical trial applications to Competent Authorities Ethics Committees and Regulatory Agencies and the research review and reporting on applicable glob

Responsible for the day-to-day activities and delivery of Global Regulatory Affairs support services. Role will include management of clinical trial applications to Competent Authorities Ethics Committees and Regulatory Agencies and the research review and reporting on applicable glob

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

The Lead Data Engineer will design build and operationalize scalable data solutions to support enterprise analytics and AI/ML initiatives. This role requires expert-level proficiency in Databricks Azure Fabric PySpark SQL and the Azure ecosystem with deep experience across data wareho

The Lead Data Engineer will design build and operationalize scalable data solutions to support enterprise analytics and AI/ML initiatives. This role requires expert-level proficiency in Databricks Azure Fabric PySpark SQL and the Azure ecosystem with deep experience across data wareho

Job Title:Clinical Data CoordinatorJob Salary: $41000 - $68000 CADJob Location:London Ontario(hybrid/remote)Reports To:Manager Clinical Data Management SupportDepartment/Unit Name:Clinical Data ManagementRole Summary: Responsible for assisting in carrying out basic clinical data manag

Job Title:Clinical Data CoordinatorJob Salary: $41000 - $68000 CADJob Location:London Ontario(hybrid/remote)Reports To:Manager Clinical Data Management SupportDepartment/Unit Name:Clinical Data ManagementRole Summary: Responsible for assisting in carrying out basic clinical data manag

Location:London OntarioJob Salary:$42000 - $70000Job Title:Image Service Coordinator (Full-time permanent)Department:Image ServicesShift Time: 12:00 - 8:00 AM ESTJob Summary:Assist in the execution of all Image Services activities ensuring focus on data integrity and reliability in ac

Location:London OntarioJob Salary:$42000 - $70000Job Title:Image Service Coordinator (Full-time permanent)Department:Image ServicesShift Time: 12:00 - 8:00 AM ESTJob Summary:Assist in the execution of all Image Services activities ensuring focus on data integrity and reliability in ac

Independently performs coordinates and oversees all aspects of the clinical site monitoring services assessing protocol and regulatory compliance as per Alimentivs and sponsors standard processes ICH/GCP guidelines and local regulation. Serves as the primary liaison between the sponso

Independently performs coordinates and oversees all aspects of the clinical site monitoring services assessing protocol and regulatory compliance as per Alimentivs and sponsors standard processes ICH/GCP guidelines and local regulation. Serves as the primary liaison between the sponso

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

Independently performs coordinates and oversees all aspects of the clinical site monitoring services assessing protocol and regulatory compliance as per Alimentivs and sponsors standard processes ICH/GCP guidelines and local regulation. Serves as the primary liaison between the sponso

Independently performs coordinates and oversees all aspects of the clinical site monitoring services assessing protocol and regulatory compliance as per Alimentivs and sponsors standard processes ICH/GCP guidelines and local regulation. Serves as the primary liaison between the sponso

Responsible for the day-to-day activities and delivery of Global Regulatory Affairs support services. Role will include management of clinical trial applications to Competent Authorities Ethics Committees and Regulatory Agencies and the research review and reporting on applicable glob

Responsible for the day-to-day activities and delivery of Global Regulatory Affairs support services. Role will include management of clinical trial applications to Competent Authorities Ethics Committees and Regulatory Agencies and the research review and reporting on applicable glob

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

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

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

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

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

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

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

The Clinical Data Analyst (CDA) is a mid-level individual contributor role that supports the Data Sciences department in identifying requirements and building solutions towards enhancing clinical study data reporting and analytics capabilities. This role will support in the developmen

The Clinical Data Analyst (CDA) is a mid-level individual contributor role that supports the Data Sciences department in identifying requirements and building solutions towards enhancing clinical study data reporting and analytics capabilities. This role will support in the developmen