Alimentiv

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...

The Sr. Vendor Manager (SVM) is accountable for the evaluation integration oversight and performance of all vendors that support Alimentivs clinical services including a wide array of central lab vendors central/local drug depots and goods and technology vendors that support e More...

The Business Development Director is responsible for the Eastern US region and supports the growth of Alimentiv business generating sales by identifying new strategic opportunities developing sales plans meeting with clients responding to requests for proposals and providing partner a More...

Responsible for developing and leading highquality strategic scalable software solutions that align with the companys goals and objectives. This role holds a strategic position within the software development lifecycle from planning to deployment and is key to shaping the technologica More...

Job Title:TMF AssociateJob Location:Toronto ON (remote)Job Salary:$52500 $87500 CADEmployment Type:Full time Limited Term (March 2025 May 2026Job Reports To:Manager TMF OperationsDepartment/Unit Name: TMF OperationsJob Summary:Responsible for the management of the Trial Master File 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...

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...

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...

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...

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...

JOB SUMMARY:Responsible for leading planning and of all data management activities for assigned projects ensuring focus on data integrity validity reliability in accordance with standard processes sponsor guidelines industry best practices and regulatory standards. Act as coach mento 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...

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...

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...

Assist with and/or complete clinical trial submissions to Regulatory Authorities Ethics Committees and other review bodies responsible for authorizing the conduct of clinical trials ensuring compliance to ICH GCP regional/local requirements. Submission support throughout the lifecycle 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...

This position will act as a Lead Database Programmer and serve as a Subject Matter Expert to internal teams and sponsors. This position will act as a mentor/trainer to new members of the team and will help lead new initiatives. This position is also responsible for undertaking the tec 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...

The Manager Process & Training Center of Excellence (PTCoE) will championoperational excellence and drive continuous process optimization within Alimentivs service delivery focusing on increasing trial efficiency speed to delivery and quality for our sponsors. This role will drive More...