Dedicated Line Manager - Clinical Project Management

Experteer OverviewIn this role you lead a team of CPMs and subsidiaries to manage project management activities that control risk, cost, schedule, and quality to meet sponsor expectations. You ensure training and development is in place and aligned with project needs. You collaborate with cross‑functional groups to drive process improvements and performance dashboards, shaping reliable delivery in clinical trials.Retribuzione / BenefitsSupervise and manage a team of CPMs and subsidiaries to ensure project milestones and deliverables are metEnsure compliance with standard processes, policies, and procedures and adherence to timelinesMaintain knowledge of EAC, baseline, and change control across scope, budget, and scheduleSet performance expectations and conduct competency reviews with direct reportsTrain and onboard new Project Management Analysts and track required trainingsDevelop and monitor project performance dashboards and ensure data accuracy in IQVIA systemsManage resource allocation/backfill to optimize utilizationProduce status and tracking reports for team and senior managementOversee invoicing processes and approvals for the teamFoster professional development and mentoring;
drive continuous improvement initiativesPartner with other functions to implement process improvementsPrepare and present team information at meetings and support department resourcing and training initiativesParticipate in functional or corporate initiativesEnsure team adherence to IQVIA core competencies and client‑focused service deliveryResponsabilitàBachelor's Degree in life sciences or related field or equivalent experience5 years clinical research experience including 3 years leadership experienceExperience in clinical project management, clinical lead management, or global trialsProven people management and mentoring abilityStrong communication and interpersonal skillsProblem solving and results‑oriented mindsetLeadership competencies in decision‑making, negotiation, and collaborationAbility to work across geographies with cultural awarenessKnowledge of clinical trials conduct and regulatory requirements (ICH GCP, local laws)Strong IT skills including MS Office and IQVIA systemsIQVIA Core Competencies awareness#J-18808-Ljbffr