At Clario, part of Thermo Fisher Scientific. Join us as a global leader in clinical trial endpoint technology and help transform evidence generation for better patient outcomes. As a Clinical Data Manager, you will review and evaluate clinical data generated from the imaging portion of sponsor clinical trials across diverse therapeutic areas, ensuring accuracy, compliance, and quality throughout the data lifecycle. 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 Perform all data management deliverables for assigned studies Attend and participate in client meetings as requested Understand requirements for study implementation and data collection Collaborate with project teams to develop study-specific edit check criteria Define, run, and review edit checks; resolve discrepant data Maintain organized, complete, and up-to-date study documentation Perform study setup including TF design, database structure, and specifications Coordinate and document receipt and processing of electronic or ancillary data from external sources Review data for errors and inconsistencies; collaborate to resolve issues Track outstanding issues and follow up until resolution Ensure CDM activities comply with regulatory guidelines Adhere to SOPs and departmental standards; assist in SOP updates Contribute to team efforts and explore opportunities to add value Maintain technical and industry knowledge through training What We Look For Bachelor’s degree in Life Sciences, or related field (or equivalent experience) 3+ years of experience in clinical data management within pharma, biotech, or CRO industry Working knowledge of relational database organization and validation Familiarity with SAS desirable Proficiency with Word, Excel, and Access preferred Understanding of clinical trial terminology desirable Strong problem-solving skills and attention to detail Ability to work independently and in a team setting; adaptable to changing priorities Excellent interpersonal and communication skills Strong documentation and organizational abilities Based in or able to work from India (remote/hybrid options available) 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.

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