Senior Manager Of Clinical Operations (Line Bardi

Senior Manager Of Clinical Operations (Line
Bardi
Emilia Romagna, Bardi

Job Overview:

We believe in harnessing science for human good.

And so we work day and night, around the world, to deliver answers for all your health questionsLabcorp Spain is looking to hire a Senior Line Manager for our Clinical Operations team.

In this position you will be based in Milan fully dedicated to our multisponsor (CDCS) division and will have some flexibility to work from home. Your main responsibilities will include:

Oversight of direct reports ((SCRA, CRA, IHCRAs & interns) by ensuring regulatory training is executed, understood and implementedIdentify and escalate issues through regular interactions with direct reports or other processesEnsures training record compliance with training matrix and ensures training records are up to dateProvide input to relevant SOPs and standard plans/templates when applicableAssist with coordination and implementation of on-boarding of new direct reports ensuring appropriate training before study-related activities beginsHold staff accountable for issue escalation to the management team, the sponsor and QA, as appropriate and determine regional implications for corrective action plansHold staff accountable for quality and compliance with project plan and adherence to contract obligations Coach staff to own effective Investigator relations and Investigator oversight Communicate status of assigned workload of direct reports for metric reportingPerform regular review of direct report billable hours and associated utilization per quarterly and annual budget plan, and escalation of outliers and assists management team for mitigationAdheres to global toolsfor monitoring and utilization forecastingEngage in Resource management activities for direct reports or across a project teamAssist with staff recruitment through screening and interviewingFinancial authority in accordance with current signature approval matrixAccountable for expense management, expense report approval and compliance with Travel Policy of direct reportsLiaise with internal and external customers in relevant process improvement initiativesEncourages use of standardized processes and tools in alignment with associated policies to ensure efficiency and productivitySupport the quality control processes to assure quality metricsSupport the department is absence of the Associate Director or Director Might be requested to work in a client facing environmentRepresent the department at client and other meetings when requestedPerform other duties as required by ManagementEducation/Qualifications:

University/college degree (life science preferred) or certification in a related allied health profession from an appropriately accredited institution (e. g. , nursing certification, medical or laboratory) Excellent level of English with capacity to effectively communicate at all levels. Experience:

+8 years direct Clinical research experience or combined with other relevant experience (i. e.

worked as a Clinical Team Leader/Project Manager at a Pharma company or CRO)+3 years supervisory experience required with demonstrated ability to lead by example and drive all required job duties or an equivalent combination of education and experience to successfully perform the key responsibilities of the job. Previous experience as a Clinical Research Associate

- This position may require some occasional travel at national level.