IQVIA
Job title:
Clinical Project Manager
Company:
IQVIA
Job description
The RoleAs Local Trial Manager you will be responsible for running international/global studies in all therapeutic areas, managing the operational aspects of projects to meet contractual requirements. You will act as primary point of contact to lead, manage and co-ordinate the conduct of clinical trials from study start-up (COLA) to close out at a country level in accordance with ICH-GCP and other applicable local regulations.RESPONSIBILITIES OVERVIEWPartner with global, local country teams and study team to provide high level country strategy, drive study progress and country level study delivery. (Accountable for study deliverables and drives key decisions within set country)Plan, manage, and maintain oversight of clinical study execution in accordance with the global program strategy, through leadership of the cross-functional Local Study Team (LST)Support country-level operational planning and accountable for site selection within assigned country(ies)Contribute and develop to program,/study-specific materials – e.g., monitoring plan, study specific training documents.Accountable for site-level goal setting and study-specific deliverables for clinical sites within their country(ies)Contribute to, deliver and/or lead CRA, Investigator and Study Coordinator trainingOversight and monitoring of applicable vendor activities e.g., laboratories and equipment provisioningContribute to the study-level forecast for investigational product, support study level accountability and reconciliation across assigned countries, management of ELE (enrolment long-range estimates) processMonitor the execution of the clinical study against timelines, deliverables, and budget for that country:Monitor and review country and study trends Review Monitoring Visit ReportsIdentify and facilitate resolution of cross-functional study-specific issuesProvide updates regarding the study budget and obtain approval for budget deviations for clinical sites (outside of range)Conducts on-site quality visits with CRAs where/when appropriate and supports the maintenance of iinvestigator site relationshipsREQUIRED EDUCATION AND EXPERIENCEBachelor’s degree in a healthcare or other scientific disciplineMinimum 2-3 years’ experience of leading local/regional or global teamsMinimum 2-3 years’ clinical trial project management experienceExperience in oversight of external vendors (e.g., CROs, central labs, imaging vendors, etc.).REQUIRED KNOWLEDGELocal knowledge / expertise of regulatory environment, study start up process and associated timelines etc.Clinical trial processes and operationsExtensive knowledge of ICH/GCP regulations and guidelinesProject and Program management including oversight of study deliverable, budgets and timelinesTime, cost and quality metrics, Key performance indicators (KPIs)Must have fluency in English, Dutch and French languagesIQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. Learn more at
Expected salary
Location
Zaventem, Brabant Flamand
Job date
Fri, 14 Jun 2024 22:35:49 GMT
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