Descripción de la oferta
Overview
In this role you drive and oversee multi-site oncology trials within a global program, acting as the primary client liaison and ensuring study delivery meets scope, quality, and budget goals. You’ll lead cross-functional teams, shape trial strategy, and support business objectives through process improvement and proactive risk management. The position offers remote work across EU/UK regions and opportunities to influence senior leadership and bid defense efforts. You will partner with clients and internal teams to deliver high-impact oncology programs.
Compensaciones / Beneficiosfully remote workwork-life balancesupportive and collaborative environmentteam developmentopportunity to influence senior leadershiptravel for bid defenses
ResponsabilidadesServe as primary client liaison and oversee client interactions, including proposals and presentationsManage all aspects of clinical trials within assigned portfolios, ensuring consistency across studiesProvide direction to project managers across study establishment, planning, execution, procurement, and closingManage study budgets, identify out-of-scope work, and drive change ordersOversee financial health: profitability, billing, and forecasting to meet business objectivesDevelop or supervise robust project plans with timelines, risk management, and change managementEnsure quality management for projects, including eTMF readiness and CAPA/quality improvementsEstablish and monitor trial and team progress metrics; prepare client and senior management status updatesLead internal and client meetings; set expectations and drive study-level strategiesOversee cross-functional teams for efficient trial execution; communicate protocol issues and corrective actionsConduct formal presentations to diverse audiences, including bid defensesEnsure study-specific training and compliance across functional areasSupport business development and travel for bid defenses; drive defense preparationMentor associate/project managers and participate in SOP updatesProvide performance feedback and address project-level issues with corrective actionsTravel domestically and internationally as required
Requisitos principales8+ years in clinical research or equivalent experience5+ years direct project management experienceProficient with Microsoft Office, Microsoft Project, eTMF, EDC, CTMSExcellent communication, interpersonal, and organizational skillsExperience managing highly complex and global studies or portfoliosMastery of ICH-GCP and relevant SOPs; strong project management techniquesCross-functional leadership abilities and stakeholder managementHigh integrity with ability to work autonomously and in teamsProven ability to plan, negotiate, and deliver on timelines and budgetsstrong communicationleadership and mentoringcross-functional collaborationMicrosoft Office (Outlook, Word, Excel, PowerPoint)Microsoft ProjecteTMF
