Clinical Project Manager
Clario · 2 Locations, India
Free account: apply link, HR contact and an AI-written cold email
Clario · 2 Locations, India
Free account: apply link, HR contact and an AI-written cold email
Join Clario, a part of Thermo Fisher Scientific, as a Clinical Project Manager supporting medical imaging programs in India. You will lead the delivery of clinical trial projects from study start-up through closeout, connecting sponsors, sites and cross-functional teams while maintaining quality, timelines, financial oversight and protocol compliance. This is an opportunity to combine clinical project leadership with work that helps bring life-changing therapies to patients faster. What We Offer Competitive compensation and incentives Provident fund and medical insurance Engaging employee programs and local events Modern office spaces and remote work flexibility What You’ll Be Doing Lead clinical study start-up activities, translating study requirements and response assessment criteria into project plans, timelines, milestones, communication plans and study documentation. Manage project execution and stakeholder communications, providing timely updates to sponsor representatives, project teams, sites, Business Development and leadership. Monitor critical project success factors, resource requirements, risks, data collection activities and overall delivery against agreed project expectations. Own key financial activities, including monthly billing, forecasting, scope reviews, amendments, pass-through costs and the project information required to support revenue reporting. Maintain strong knowledge of project contracts, study protocols and Standard Operating Procedures (SOPs), partnering with Quality Assurance to address deviations and communicate protocol updates. Lead, train and support cross-functional project teams, establishing clear project expectations and partnering with functional leaders on coaching and development. Support Business Development activities through capabilities discussions, sponsor meetings and polished Investigator Meeting presentations. Coordinate study closeout and applicable submission activities, ensuring project deliverables are completed appropriately. Where applicable, provide people-management support, including setting expectations, coaching, performance management, hiring and onboarding. What We Look For Bachelor’s degree or equivalent practical experience; education in life sciences, pharmacy, nursing or another healthcare field is highly desirable. 1–3 years of clinical trials experience within a contract research organization (CRO) or pharmaceutical research environment, preferably in project management. Previous project or management experience supporting the clinical development of investigational medicines. Working knowledge of Good Clinical Practice (GCP), International Council for Harmonisation (ICH) guidelines and relevant clinical research regulations. Medical imaging experience is preferred. Experience with common project and business productivity tools, including Microsoft Word and Excel; Microsoft Project experience is preferred.
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