Associate Data Team Lead

Hace 2 días

Madrid, España IQVIA Jornada completa
Experteer Overview As an Associate Data Team Lead, you will independently drive end-to-end data management delivery for large, global studies, ensuring quality, timeliness, and customer satisfaction. You’ll lead CDM activities, mentor junior staff, and partner with clients and internal teams to manage scope, budget, and process improvements. The role blends project leadership with SME-level DM expertise to advance data integrity across programs. This is a remote, client-facing leadership opportunity within IQVIA’s CDM organization. Compensaciones / Beneficios
• Lead end-to-end data management delivery for multiple/global studies
• Serve as primary client contact for data deliverables and maintain strong customer relationships
• Provide project management oversight, including planning, risk management, and issue escalation
• Lead negotiations on timelines, cost, and resources; manage SOWs and budgets
• Sign-off on data management plans (DMPs) and ensure adherence to contracts/SOWs
• Coach and mentor junior DTL staff; train on DM expertise
• Act as SME for CDM tasks or technologies; coordinate cross-functional DM activities
• Implement proactive quality management across projects and drive process improvements
• Serve as escalation point for data issues; coordinate resolutions with clients and vendors
• Support RFP processes and participate in bid defenses
• Maintain internal tracking systems and support service delivery improvements
• Represent the team in CDM workshops and contribute to SOPs and WG initiatives Responsabilidades
• 7 years direct DM experience, including 5+ years as a CDM lead
• Experience delivering multiple global trials through full DM life-cycle (large trials, u003e=1000 patients)
• Strong background in DM processes (SAE reconciliation, external vendor reconciliation, local lab data, new technology)
• Proven experience in complex client negotiations and bid defenses
• Knowledge of Medical Terminology, Pharmacology, Anatomy/Physiology
• Knowledge of GCPs and regulatory guidelines
• Excellent communication, interpersonal, and teamwork skills
• Strong project management and problem-solving abilities
• Ability to work independently and manage cross-functional teams
• Understanding of the clinical drug development process Requisitos principales
• remote work
• autonomy in a fully remote role
• global collaboration with a cross-functional team