Requirements: English
Company: IQVIA Italia
Region: Lombardy
On behalf of our client, a global pharmaceutical company, IQVIA is seeking a Vendor Management Lead for Drug Development. This role involves overseeing the selection, contracting, oversight, and performance management of external vendors and collaborators based in Italy, supporting clinical development. External vendors include CROs, CMOs, central labs, and bioanalytical labs, while external collaborators comprise academic and clinical researchers.ResponsibilitiesCollaborate with internal and external stakeholders across clinical, regulatory, project management, and other functional areas to advance activities in Italy, other European countries, and potentially other regions.Identify and assess CROs, CMOs, central labs, specialty vendors, and other service providers.Lead RFI and RFP processes, evaluating vendors based on capabilities, compliance, cost, and timelines.Oversee site selection, recruitment, and monitoring activities for clinical trials within Italy.Work closely with quality teams to ensure vendor compliance with GCP, GMP, GLP, ICH guidelines, and company policies.Manage external service providers, ensuring all deliverables are met.Facilitate seamless vendor integration into drug development programs and inter-vendor processes.Assist Program Management in developing and managing budgets and timelines, and track key metrics and performance indicators.Implement CAPAs when performance gaps occur.Review purchase orders, invoices, and perform financial reconciliation with finance teams.Provide vendor-related insights for regulatory submissions and inspection readiness.Represent the company at vendor meetings and conferences as needed.QualificationsBachelors degree in Life Sciences or a related field; Masters or PhD preferred.At least 5 years of clinical operational experience in pharma, biotech, or medical devices, with a minimum of 2 years in vendor management.Experience managing CROs, CMOs, bioanalytical labs, and clinical technology vendors.Knowledge of clinical trial design, execution, and regulatory requirements (GCP, ICH, FDA, EMA).Strong leadership, project management, and communication skills.Fluency in English and Italian (written and spoken).Additional Skills & CompetenciesAttention to detail and ability to manage multiple complex projects.Proactive problem-solving and cross-functional collaboration skills.Excellent interpersonal, communication, and organizational skills.Proficiency with CTMS and Microsoft Office Suite.Employment Requirements in ItalyAbility to work under an open-ended, part-time or full-time contract, depending on company needs.BenefitsCompetitive salary package based on experience.Health insurance and pension contributions.Paid time off and public holidays.Professional development opportunities.Flexible working arrangements (subject to company policies).#J-18808-Ljbffr