Alimentiv

Acts as the primary regional representative for the 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 meet spons More...

In conjunction with the Senior Manager People & Culture the Human Resources Business Partner (HRBP) is responsible for planning aligning and implementing the organizations human resource strategy to the assigned product lines/departments to achieve their current and future busine More...

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 scale. Inhouse based position responsible for the design and oversight of project monitoring services in More...

Responsible for the successful planning management change control and delivery of numerous concurrent complex infrastructure and computer system projects within the IT Department and across Alimentiv Product Lines following Project Management Institute (PMI) Project Management Profe More...

We are seeking a highly skilled Product Manager to lead the development and enhancement of our innovative Clinical Data Management System (CDMS) for Medical Imaging in clinical trials. The ideal candidate will have a strong technical background in Computer Science or Engineering comp More...

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 manage More...

As a Product Support Specialist you serve as a link between user feedback and actionable solutions. This role will work crossfunctionally to help our frontline Image Services (Service Desk) team supporting clinical research sites Sponsor facing Project Management teams and the interna More...

This is an exciting opportunity to join a growing stateof theart CAP/CLIA accredited laboratory focused on accelerating biomarker and drug development. You will have the opportunity to apply your knowledge and gain more experience in the areas of anatomic and molecular pathology. More...

Responsible to plan manage organize evaluate and/or report on the daytoday delivery of the Financial Planning & Analysis unit in collaboration with Sr. Director Financial Planning & Analysis. As part of the management in the department participate in the development and implem More...

Responsible for the daytoday 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 global More...

Support Project Management Regulatory and Contract and Legal in all siterelated startup activities. Establish relationships with study personnel at sites and act as main Alimentiv contact during site startup. Prepare distribute and followup on startup documents with sites. Plan and tr More...

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 scale. Inhouse based position responsible for the design and oversight of project monitoring services in More...

Acts as the primary regional representative for the 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 meet spons More...

As the primary sponsor liaison and advocate the Clinical Project Manager will plan execute manage and monitor regional single modality or therapeutic area clinical research projects. Utilizing existing templates processes and programs as a guide he or she will adapt/develop implement More...

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) IC More...

As the primary sponsor liaison and advocate the Clinical Project Manager will plan execute manage and monitor regional single modality or therapeutic area clinical research projects. Utilizing existing templates processes and programs as a guide he or she will adapt/develop implement More...

Job Title: Administrative GeneralistJob Location:Poland Job Type: Fulltime PermanentDepartment/Unit Name:Full Service Clinical Project ManagementProvide administrative support and assistance to the department and/or Director to facilitate efficient operation according to project corp More...

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 subjec More...

Support Trial Master File (TMF) activities to ensure TMFs are inspection ready throughout study lifecycle and TMF documents are filed contemporaneously. Primarily responsible for document attribute review processing tracking and filing; and paper and/or electronic folder creation. Ser More...

Provide administrative support and assistance to the department and/or Director to facilitate efficient operation according to project corporate industry and regulatory guidelines and standards. Responsible for the daytoday management of paper and electronic documents including review More...