Join Clario, a part of Thermo Fisher Scientific and help shape the delivery of innovative electronic Clinical Outcome Assessment (eCOA) solutions that support clinical trials around the world. As a Project Manager within our eCOA business unit, you will lead cross-functional project teams through the successful execution of global clinical studies, ensuring high-quality delivery, exceptional customer service, and adherence to project timelines and budgets. You will serve as a trusted partner to sponsors and internal stakeholders, driving study success from startup through closeout while helping bring life-changing therapies to patients faster. This India-based role supports global customers and project teams and may require flexibility to collaborate across multiple time zones, including regular coverage of U.S. stakeholder meetings when needed. What We Offer • Competitive pay and incentives. • Provident fund and medical insurance. • Engaging employee programs and local events. • Modern office spaces and remote work flexibility. • Opportunities for professional growth and career development within a global organization. What You'll Be Doing • Lead the planning, setup, monitoring, and closeout phases of eCOA studies and programs. • Gather customer requirements and translate study needs into actionable plans for cross-functional operational teams. • Develop, maintain, and manage study documentation throughout the project lifecycle. • Coordinate the distribution, tracking, reconciliation, and management of study devices and associated equipment. • Create, review, and distribute study status reports, metrics, and project communications. • Ensure appropriate archival of study data, documentation, and project records in accordance with company and regulatory requirements. • Establish and manage customer expectations through proactive communication and effective stakeholder engagement. • Monitor study timelines, milestones, deliverables, and dependencies to ensure successful project execution. • Manage financial aspects of assigned studies, including budget reviews, revenue forecasting, scope change assessments, and invoice reconciliation activities. • Identify project risks, develop mitigation strategies, and escalate issues appropriately to support study success. • Facilitate collaboration between sponsors, vendors, and internal teams to drive efficient use of resources and achievement of contractual obligations. • Lead internal and external discussions, negotiations, and stakeholder communications to support successful study execution. • Apply structured problem-solving methodologies to address customer concerns and project challenges. • Maintain issue tracking documentation and ensure timely follow-up and resolution of customer escalations. • Serve as the Project Management point of contact for operational readiness activities related to new product and service initiatives. • Present eCOA services and operational workflows during investigator meetings, site initiation meetings, and client presentations as required. • Support onboarding, mentoring, and training of new Project Management team members. • Contribute to departmental initiatives, process improvements, and special projects as assigned. What We Look For • Bachelor's degree or equivalent combination of education and relevant project management experience. • 1 to 4 years of project management experience within pharmaceutical, biotechnology, healthcare, clinical research, life sciences, or related industries. • Understanding of the drug development process and clinical trial environment. • Experience supporting technology-enabled clinical trials, eCOA, ePRO, eConsent, RTSM/IRT, or related eClinical solutions is preferred. • Strong project planning, organization, prioritization, and time management skills. • Experience coordinating multiple stakeholders, timelines, budgets, and deliverables simultaneously. • Knowledge of project financial management concepts, including budgeting, forecasting, invoicing, and scope management. • Strong risk management and problem-solving skills with the ability to proactively identify and address project challenges. • Excellent verbal and written communication skills with the ability to communicate effectively in English. • Strong interpersonal skills and the ability to build productive relationships with sponsors, sites, and cross-functional teams. • Working knowledge of Microsoft Office applications, including Excel, PowerPoint, Word, Outlook, and Teams. • Detail-oriented with demonstrated responsiveness to customer inquiries and operational requests. • PMP certification preferred. At Clario, a part of Thermo Fisher Scientific, our purpose is to transform lives by unlocking better evidence. It’s a cause that unites and inspires us. It’s why we come to work—and how we empower our people to make a positive impact every day. Whether you're advancing clinical science, building innovative technology, or supporting our global teams, your work helps bring life-changing therapies to patients faster.