Senior Manager - Full Stack Developer- Clinical Data Operation

About Regeneron Regeneron is founded on the belief that the right idea, combined with the right team, can lead to significant transformations. Our growing global network is dedicated to inventing, developing, and commercializing medicines that change lives for those with serious diseases. In doing so, we are pioneering innovative approaches to science, manufacturing, and commercialization, as well as redefining our understanding of health. As a Senior Manager – Clinical Data Solutions & Insights, you will be responsible for designing, building, and handling a centralized clinical reporting platform that consolidates reporting outputs across Data Management and external vendor reconciliation activities into a single governed reporting layer. This role will be responsible for the end-to-end reporting lifecycle including data ingestion, analytical dataset development, dashboard creation, automated reporting, and self-service analytics applications using modern visualization and web technologies. You will work closely with Clinical Sciences, Data Management, Pharmacometrics, Precision Medicine, Safety, and multi-functional collaborators to deliver intuitive, audit-ready reporting solutions that support data-driven decision making, regulatory compliance, and operational perfection. This position is office-based and will be on site at Regeneron's Hyderabad office. A Typical Day May Include: Owning the design and delivery of a centralized clinical reporting platform consolidating EDC listings, exception reports, and vendor reconciliation outputs Building and maintaining Clean Patient Tracker applications providing real-time access to CRF completion, visit status, data queries, freeze/lock status, and PI signature status Developing executive-level dashboards highlighting portfolio-wide KPIs such as query aging, protocol deviations, data entry lag, and study completion achievements Partnering with Data Management Reporting teams and external vendor delivery teams to establish structured data ingestion pipelines for EDC and reconciliation reports Collaborating with Clinical Sciences, Biostatistics, Safety, and Precision Medicine teams to develop validated self-service analytical tools and reporting applications Designing and implementing data visualization standards, UX/UI guidelines, and reporting procedures for non-technical stakeholders Building curated analytical datasets and semantic layers connected to clinical data lakes and vendor reconciliation feeds Running the full reporting lifecycle including requirements gathering, UX wireframing, development, validation, UAT coordination, and production deployment Driving automation across routine reporting workflows including scheduled data ingestion, reconciliation report generation, and alert-based notifications Supporting GCP compliance, inspection readiness, report governance, version control, and audit trail management Driving adoption of reporting tools through stakeholder engagement, training, and change management initiatives Serving as an SME for clinical data reporting, embedded analytics, and emerging visualization technologies This Role May Be For You If You Have: Demonstrable experience in Clinical Data Management, clinical trial reporting, analytics, or reporting platform development Hands-on experience with Medidata Rave EDC including query management workflows and dataset structures Solid understanding of CDISC CDASH/SDTM standards and GxP/CSV validation principles Experience developing reporting applications using Python frameworks such as Dash, Streamlit, or Flask Demonstrable experience with Power BI, Tableau, SQL, and analytical dataset development Experience working with clinical data sources, clinical metrics, and external vendor reconciliation outputs Strong UX/UI design sensibility for building intuitive reporting tools for non-technical users Excellent stakeholder management, communication, and presentation skills Strong analytical thinking and problem-solving capabilities Ability to work optimally in a fast-paced, matrixed, and multi-functional environment To Be Considered For This Role, You Must Have: 8+ years of experience in Clinical Data Management or clinical trial operations Minimum 3+ years focused on clinical data reporting, analytics, or reporting tool development Experience with clinical reporting applications, dashboards, and data visualization tools Bachelor's or Master's degree in Computer Science, Data Science, Bioinformatics, or a related field Advanced degree (MBA/MS) preferred Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries' specific benefits, please speak to your recruiter. Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron's roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron's on-site policy and expectations for your role and your location. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business. For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location. Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc. Regeneron is a leading biotechnology company that invents life-transforming medicines for people with serious diseases. Founded and led for over 30 years by physician-scientists, our unique ability to repeatedly and consistently translate science into medicine has led to nine FDA-approved treatments and numerous product candidates in development, almost all of which were homegrown in our laboratories. Our medicines and pipeline are designed to help patients with eye diseases, allergic and inflammatory diseases, cancer, cardiovascular and metabolic diseases, neurology, infectious diseases and rare diseases. Regeneron is also proud of award winning culture of innovation, being recognized as a Great Place to Work in 2021, Fast Company's Best Workplace for Innovators in 2020, and Forbes JUST companies in 2020, among others.