Clinical Program Manager

Clinical Program Manager - Project Planning & Program Coordination (Sponsor Dedicated)Join to apply for the Clinical Program Manager - Project Planning & Program Coordination (Sponsor Dedicated) role at IQVIA.This position will primarily support Global Program Leaders (GPLs) in managing a Clinical Team to meet deliverables outlined in the CompoFund Development Plan (CDP). The role involves understanding the drug development process to deliver a clinical program according to quality, timelines, and budget in close partnership with the GPL, the Clinical leader, and the Project Management Lead (PML) at the Clinical Development Team (CDT) level. Key responsibilities include managing external partners, facilitating stage gate activities for TA governance, coordinating clinical supplies, addressing urgent safety measures, and supporting financial and timeline planning.ResponsibilitiesDevelop initial high‑level study cost estimates for new study concepts to support early planning and decision‑making.Partner with TDLs and TDMs to ensure timelines, resources, and operational drivers are accurately represented in planning tools (PLW).Provide portfolio‑level insights and narratives to senior management (TA Leads, PDLs) to inform strategic decisions.Create, manage, and maintain study schedules in PLW for sponsored and collaborative studies; support OOPs management through First Patient In (FPI).Ensure clinical timelines in PLW align with mCTMS and latest assumptions; reflect proper resource demand.Develop budget, timeline, and FTE forecasting scenarios in PLW, including situational operational scenarios.Collect, consolidate, and report financial, timeline, and resource data for governance approvals and external funding partnerships; manage scope control, FTE, and OOP variances.Provide portfolio data insights to TA Leads and PDLs for governance and strategic planning.Support Finance, Business Partners, and Commercial stakeholders with accurate data and operational inputs.Adhere to applicable Sponsor SOPs, WIs, policies, local regulatory requirements, etc.Manage Clinical Team (CT) agendas, documentation, and communications to ensure timely and accurate dissemination of the CT strategy and operational status throughout the cross‑functional team and with co‑development partners or other external partners.Partner with the GPL and GTL, program coordinators, and Finance to support continuous forecasting for the program under that Clinical Team.Partner with cross‑functional leads within and outside Global Development (e.g., regulatory, finance, clinical supplies, Biomarker departments, Global Medical Safety) to ensure appropriate communication and risk/escalation resolution around quality, timelines, and budget.Manage governance infrastructure and reporting with co‑development partners and other external partners as directed by the GPL.RequirementsBS degree or equivalent in Life Sciences (e.g., Biology, Chemistry, Biochemistry, Nursing, Pharmacy).6‑8 years clinical trial management experience in the pharmaceutical industry or CRO; specific therapeutic area experience.Strong knowledge of ICH‑GCP, local laws, and regulations.Demonstrated operational knowledge of clinical research; proven track record managing trials from start‑up to database lock and closure.Effective leadership to drive the Study Management Team through key trial stages and delegation.Ability to manage multiple stakeholders and lead a high‑performing team.Experience coordinating global or regional teams in a virtual environment (minimum 2–3 years).Proactive planning, risk mitigation, and team consensus building throughout the project lifecycle.Strong project planning/management and independent complex decision‑making skills.Solution‑oriented risk identification and mitigation.Strong IT skills, including Microsoft applications, Trial Master File, Clinical Trial Management System; willingness to learn new systems.Monitoring experience preferred; other relevant experience (data management, central monitoring) considered.Proficient in speaking and writing local country language and English.Effective verbal and written communication skills leading to successful collaboration.Strong analytical skills and ability to manage ambiguity with limited information.Experience developing presentations and presenting key information to stakeholders.Understanding and oversight of country budgeting processes, including OOPs and FTE cost drivers.IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com #J-18808-Ljbffr