Data Manager

Join Clario, part of Thermo Fisher Scientific, as a Data Manager within our Digital Physiology team. You will play a key role in ensuring high‑quality data is collected, processed, and delivered to Sponsors across global clinical studies. You will act as the primary point of contact for data‑related activities, working closely with internal teams, Sponsors, and CRO partners to ensure data integrity, compliance, and timely delivery. What We Offer Competitive compensation Comprehensive health, dental, and vision coverage Retirement savings plan with company contribution Paid time off and company holidays What You’ll Be Doing Serve as the primary internal and Sponsor contact for all Data Management questions, issues, and escalations related to data collection, cleaning, delivery, reconciliation, timelines, and database lock Define, maintain, and communicate the Data Management Plan (DMP) in collaboration with Sponsors and internal Clinical Data Management teams Determine and document standard and study‑specific edit checks and data processing guidelines to ensure clean, high‑quality data Collaborate with internal teams on study setup requirements, including demographics collection and visit schedule requirements Lead the development, review, and finalization of data transfer requirements, including file specifications and approvals Coordinate with SAS Programmers for data file creation, edit check development, and validation activities Generate and deliver sample, routine, complete, and final data transfers in line with study timelines Manage database lock activities with Sponsors to ensure data integrity and deliverable timelines are met Act as the primary point of contact for Data Correction Requests (DCRs) and query escalation Participate in the review and approval of Data Management components to ensure high‑quality study setups Maintain complete and up‑to‑date Data Management documentation, including Data Management Plans, file specifications, data transfer agreements, data correction requests, and Sponsor communications Identify out‑of‑scope requests and escalate to the Project Manager for Change Order processing Conduct routine status meetings with Sponsors, CROs, and internal teams, including preparation of agendas and meeting minutes Support monthly reporting activities by providing Data Management metrics as required Deliver high levels of customer satisfaction by meeting commitments, timelines, and quality expectations What We Look For Bachelor’s degree in Life Sciences or a related field preferred Minimum of 2 years of Data Management or related experience, preferably within a clinical research environment Prior client‑facing experience preferred Proficiency in Microsoft Office applications Strong organizational, time‑management, interpersonal, and problem‑solving skills Ability to manage multiple priorities in a fast‑paced, regulated environment High attention to detail and commitment to data quality Exposure to or experience with SAS and/or SQL is a plus Knowledge of CDISC SDTM standards is a plus Strong written and verbal communication skills in English At Clario, 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. 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.