Assistant Clinical Project Manager

Clario, a part of Thermo Fisher Scientific, is the global leader in medical imaging, providing expert services and technology to support clinical trials across the drug development lifecycle. Within our industry‑leading Medical Imaging division, we support some of the most complex Oncology studies worldwide. We are currently seeking an Assistant Clinical Project Manager (ACPM) to support the successful delivery of imaging‑based clinical trials from our India operations. This role offers exposure to global studies, cross‑functional collaboration, and the opportunity to build a strong foundation in clinical project management within a regulated, fast‑paced environment. 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 What You’ll Be Doing Support Clinical Project Managers (CPMs) with day‑to‑day project administration across study start‑up, execution, and close‑out activities Develop, review, and edit project documentation, presentations, and reports Read, understand, and apply clinical protocols and imaging requirements to project activities Participate in project meetings, client calls, and internal training sessions Act as a liaison across cross‑functional teams to ensure timely completion of study deliverables Monitor internal data flow to ensure tasks are completed within agreed timelines Track outstanding items such as missing data, queries, or incomplete documentation and follow up to resolution Communicate project status updates to clients and internal stakeholders in a professional and timely manner Support logistics activities, including distribution, tracking, and management of site‑facing materials Assist with finance‑related activities such as scope change documentation, database updates, invoice reconciliation follow‑ups, and forecasting reports Create, review, and distribute internal and external project reports Serve as acting Project Manager during temporary CPM absence, as required What We Look For Associate’s degree required; Bachelor’s degree preferred 2+ years of experience in pharmaceutical drug development, clinical trials, or clinical research (preferred) Strong working knowledge of Microsoft Office (Word, Excel, PowerPoint, Outlook) Healthcare, medical imaging, or clinical research exposure preferred Excellent written and verbal communication skills in English Strong organizational, time management, and prioritization skills Detail‑oriented, responsive, and able to manage multiple priorities Ability to work independently while collaborating effectively in a team environment Comfortable working in a dynamic, changing environment with a proactive and pragmatic approach At Clario, 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. Clario Privacy Policy Clario is a leading provider of endpoint data solutions to the clinical trials industry, generating high-quality clinical evidence for life sciences companies. We offer comprehensive evidence generation solutions that combine medical imaging, eCOA, precision motion, cardiac solutions and respiratory endpoints. For more than 50 years, Clario has delivered deep scientific expertise and broad endpoint technologies to help transform lives around the world. Our endpoint data solutions have supported over 30,000 clinical trials in more than 100 countries. Our global team of science, technology, and operational experts have supported over 70% of all FDA drug approvals since 2015.