Senior Manager - Full Stack Developer- Clinical Data Operation

Regeneron India Private Limited; Hyderabad; On-site; INR 1,500,000 - 2,000,000; Full time

Benefits offered by this job

Health and wellness programs

401(k) company match

Annual bonuses

Paid time off

Job summary

Regeneron India Private Limited is seeking a Senior Manager – Clinical Data Solutions & Insights to design and manage a centralized clinical reporting platform at our Hyderabad office. This role will involve overseeing data ingestion, analytics, and the development of intuitive dashboards.

The ideal candidate is expected to have over 8 years of experience in Clinical Data Management and strong expertise in reporting tools and analytics. Experience with Python frameworks and stakeholder engagement is essential.

Qualifications

• 8+ years of experience in Clinical Data Management or clinical trial operations.
• 3+ years focused on clinical data reporting, analytics, or reporting tool development.
• Hands-on experience with Medidata Rave EDC including query management workflows.

Responsibilities

• Design and deliver a centralized clinical reporting platform.
• Develop executive-level dashboards highlighting portfolio-wide KPIs.
• Drive automation across routine reporting workflows.

Skills

Clinical Data Management

Analytics

Stakeholder Management

Python frameworks (Dash, Streamlit, Flask)

Power BI

Tableau

SQL

UX/UI Design

Analytical Thinking

Communication skills

Education

Bachelor’s or Master’s degree in Computer Science, Data Science, Bioinformatics, or a related field

Advanced degree (MBA/MS) preferred

Tools

Medidata Rave EDC

CDISC CDASH/SDTM standards

Job description

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.

Typical Day

• 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

Job Requirements

• 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

Minimum Qualifications

• 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

Benefits

We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits include health and wellness programs (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 (military and parental leave) for all eligible employees. For additional information about Regeneron benefits in the US, see https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter. Many Regeneron roles are required to be performed on‑site; please discuss on‑site policy and expectations with your recruiter and hiring manager.

Equal Opportunity Employer Statement

Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. 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.