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 guidelines and local regulations. The COL acts as a primary liaison between the CRAs and the clinical project team. Additional responsibilities include project specific training of CRAs, conducting assessment visits with CRAs, implementation of enrollment and recruitment strategies, preparation of the monitoring plan and other structural documentation and the oversight of monitoring visit scheduling, site and monitoring performance metrics, issue escalation and corrective actions. The COL will develop study tools for site and CRA use, review visit reports, review and track protocol deviations, and support other objectives for clinical operations and the clinical project team.
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- nOverall oversight of (a group of) regional CRAs to ensure (site) compliance with study protocol, study plans, ICH-GCP, local regulations and study timelines.
- nMonitoring support visits (Co-monitoring), per project requirements, to aid the site/CRA in the satisfactory performance and compliance with standards mentioned above.
- nMay support clinical project team by providing oversight of study deliverables related to other departments (e.g. Data Management, TMF Operations, etc.)
- nOversee regional startup and feasibility activities.
- nAssist in vendor management activities as required per project.
- nPerform review of visit reports for quality, compliance and appropriate site management.
- nAssure compliance with high quality and timely project deliverables according to the project requirements and the monitoring plan.
- nProactive management of site and country performance (recruitment, data collection, document collection, TMF review etc.) and inform clinical project team on progress.
- nContribute to financial project management processes as applicable. May include but may not be limited to input on revenue recognition, site payments, and site pass-through expense review.
- nMay be required to manage/oversee investigator sites including CRA responsibilities, on a temporary or permanent basis.
- nConduct regular global CRA calls with the monitoring and site management team, as well as individual/country CRA calls
- nAttend meetings with Study Sponsor to provide status updates on country and site progress
- nProvide operational support and guidance to the monitoring team throughout project.
- nProvide project training/mentoring to regional CRAs on study procedures, clinical plans and guidelines, and timelines for the study. Ensures study specific training requirements are completed and documented.
- nFirst point of contact for regional CRAs for study-specific questions and issues. Escalates to PM and other functions as appropriate.
- nSupport line managers by providing status updates on utilization and performance of CRAs.
- nLiaise with line manager for assigning sites to CRAs following line manager allocation of a CRA resource to the project.
- nConduct CRA Assessment visits per departmental requirements to assess the performance of the CRA against their monitoring responsibilities.
- nDevelop training materials and study tools for sites and CRAs, including monitoring plans.
- nDevelop and implement enrolment and recruitment strategies together with clinical project team.
- nDevelop presentation materials for and presents at Sponsor Kickoff meetings, Investigator meetings and Sponsor Calls (as needed), and prepares presentations for Site Qualification Visits and Site Initiation Visits.
- Fluent in the reading, writing, and speaking of English
- nUndergraduate university degree (Bachelors or Honors Bachelors) AND 4-6 years experience + substantial on-going job-related trainingn
- nHealth Sciences, Life Sciences or Nursing specialty preferred, or SoCRA and/or ACRP Certification/Designation.
- nShould have a minimum of 3 years CRA experience, have strong experience with EDC systems, be proficient with MS Office, have strong written and verbal communication skills and highly effective interpersonal and organizational skills.n
- Demonstrate the following attributes: proactive, detail oriented, task-driven and highly organized.n
- Demonstrate the critical elements of GCPs and local regulations as they relate to clinical monitoring, IRB/EC and Investigator responsibilities.n
- Demonstrated ability in report writing and strong ability to critically understand clinical research documents.n
- Ability to handle multiple tasks to meet deadlines in a dynamic environment.
nAccommodations for persons with disabilities are available on request in respect of all aspects of the recruitment and selection lifecycle. Requests can be directed to [Confidential Information]
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