Our Sponsor Dedicated (cFSP) team is growing and weare looking for aspiring CRAs of all levels, join us on our missionto drive healthcare forward!What We Offer / USPsThe chance to workon cutting edge medicines at the forefront of new medicinesdevelopmentIQVIA has access to significant data pools allowingbetter site selection and recruitment. This helps drive performanceof sites making the CRA role more efficient and discussions at sitemore productive. Next generation clinical development!We offergenuine career development opportunities for those who want to growas part of the organizationWe invest in keeping our teams stable,so workload is consistentWe can offer flexibility regarding sitelocations to minimize travel. We can also consider candidateslooking for a 4 day working weekAs a CRA you will receive an iPadand use of key developments such as site visit app’s, site visitreport app’s that allow CRA’s to do their day job moreefficientlyResponsibilitiesPerform site monitoring visits(selection, initiation, monitoring and close-out visits) inaccordance with contracted scope of work and regulatoryrequirements, i.e., Good Clinical Practice (GCP) and InternationalConference on Harmonization (ICH) guidelinesWork with sites toadapt, drive, and track subject recruitment plan in line withproject needs to enhance predictabilityAdminister protocol andrelated study training to assigned sites and establish regularlines of communication with sites to manage ongoing projectexpectations and issuesEvaluate the quality and integrity of studysite practices related to the proper conduct of the protocol andadherence to applicable regulations. Escalate quality issues asappropriateManage the progress of assigned studies by trackingregulatory submissions and approvals, recruitment and enrollment,case report form (CRF) completion and submission, and data querygeneration and resolution. May support start-up phaseEnsurecopies/originals (as required) site documents are available forfiling in the Trial Master File (TMF) and verify that theInvestigators Site File (ISF) is maintained in accordance with GCPand local regulatory requirementsCreate and maintain appropriatedocumentation regarding site management, monitoring visit findingsand action plans by submitting regular visit reports, generatingfollow-up letters and other required study documentationCollaborateand liaise with study team members for project execution support asappropriateIf applicable, may be accountable for supportingdevelopment of project subject recruitment plan on a per sitebasisIf applicable, may be accountable for site financialmanagement according to executed clinical trial agreement andretrieve invoices according to local requirementRequirementsYoushould be life science degree educatedYou have experience ofindependent on-site monitoring experienceYouve handled multipleprotocols and sites across a variety of drug indicationsFlexibilityand ability to travelStrong communication, written and presentationskillsAwardsFORTUNE Magazines Worlds Most Admired Companies listfor the fourth year in a row - Ranked #1 in Its Category for theSecond Consecutive YearBest AI-based Solution for Healthcare” Awardin 2023 Artificial Intelligence Breakthrough AwardsThis role is noteligible for UK visa sponsorshipIQVIA is a leading global providerof clinical research services, commercial insights and healthcareintelligence to the life sciences and healthcare industries. Wecreate intelligent connections to accelerate the development andcommercialization of innovative medical treatments to help improvepatient outcomes and population health worldwide. Learn more athttps://jobs.iqvia.com