Full-Time

Senior Study Start-Up Specialist

Site Start-Up Planning and Tracking, Project Management Support

Posted on 9/9/2025

Alimentiv

Alimentiv

Compensation Overview

CA$78k - CA$130k/yr

Toronto, ON, Canada

Remote

Category
Medical, Clinical & Veterinary (1)
Requirements
  • Undergraduate degree (Bachelor’s or Honours Bachelor’s) with minimum 4–6 years of relevant experience
  • Bilingual in French/English strongly preferred
Responsibilities
  • Lead the site identification to site activation on Full Service and/or Medical R&D Clinical Trials
  • Develop and utilize intelligence databases and tools to identify the ‘best fit’ sites for a study
  • Establish relationships with study personnel at sites and act as the main Alimentiv contact during site start-up
  • Prepare, distribute and follow-up on start-up documents with sites
  • Plan and track site start up activities using designated systems and tools
  • Identify and initiate best practices, reports on intelligence and metrics related to study start-up activities
  • Oversee Startup Specialist/s that may additionally support the study
  • Provide guidance, tools, and best practices to support Project Management to drive faster study startup
  • Develop and maintain relationships with study team and sites to facilitate timely completion of start-up activities
  • Proactively plan priorities with the collection of site essential documents based on regulatory submissions and approvals
  • Track progress of startup activities and provide status reports on an ongoing basis
  • Contact and collect feasibility data from sites working closely with contracts and legal
  • Ensure that sites move through the feasibility process promptly, tracking each step and identifying risks to start-up timelines
  • Contribute to the identification and initial feasibility of new sites
  • In cooperation with Project Management and Regulatory Affairs create study-specific start-up document package
  • Distribute and follow up with sites to obtain the required executed documents
  • Review content and correctness of returned documents from the sites, in accordance with internal standards
  • In conjunction with Regulatory Affairs, ensure that the correct and complete packages are obtained within the planned timelines
  • Support Regulatory and sites with local EC site submission packages, tracking of document versions and approvals, when required
  • Act as main point of contact for sites to obtain feedback on budget and contract negotiations
  • In conjunction with the Project Manager, create and provide sites with the suggested study budget and negotiate within pre-approved margins
  • Contribute to the development of the site contracting and site budget intelligence databases
  • Ensure essential document package for IP release is complete and signed
  • Oversee the tracking of pre-site activation activities working with Project Management, CIMS, Monitoring and Site Management
  • Contribute and maintain the study startup intelligence databases
  • Identify process improvements, updates to quality and guidance documents
  • Contribute to new innovations introduced to improve and expedite the site startup process
  • Providing guidance/mentorship/support to more junior members of the team

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INACTIVE