Specialist, Clinical Data Reporting

Regeneron Pharmaceuticals, Inc; Hyderabad; Hybrid; INR 800,000 - 1,200,000; Full time

Job summary

Regeneron Pharmaceuticals, Inc is looking for a Specialist, Clinical Data Reporting in Hyderabad. In this hybrid role, you will support clinical trial oversight and produce accurate reporting outputs that drive essential data cleaning and decision-making.

The ideal candidate should possess at least 2 years of relevant experience in clinical data, alongside a Bachelor's or Master's degree in a suitable field. You'll need proficiency in EDC systems and data visualization tools to thrive in this role.

Qualifications

• 2+ years of experience in clinical data or data visualization.
• Experience with building interactive reporting solutions.
• Strong understanding of clinical data standards and regulatory requirements.

Responsibilities

• Program and maintain standardized clinical data reports.
• Translate study reporting requirements into specifications.
• Monitor routine data refreshes and troubleshoot issues.
• Communicate clearly with cross-functional partners.

Skills

Clinical data management

Data visualization tools

Clinical trial processes

Proficiency in EDC systems

Automation

Education

Bachelor's or Master's degree in Data Science, Computer Science, Life Sciences or related field

Tools

SAS

R

Python

Tableau

Power BI

Job description

Build our future together

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.

At Regeneron, we use science and innovation to develop life‑changing medicines for people with serious diseases. We are seeking a Specialist, Clinical Data Reporting to join our Data Management team, supporting clinical trial oversight and study‑level data review in a hybrid role. In this role, you will produce accurate and consistent reporting outputs that drive data cleaning, medical review, and operational decision‑making, while collaborating with clinical data management, technology partners, and cross‑functional teams to deliver study‑level reports on schedule. This position offers the opportunity to contribute to a fast‑growing, science‑driven organization making a meaningful difference to patients worldwide.

When & where:

Hyderabad, India (hybrid)

Discover your role:

• Program and maintain standardized clinical data reports and listings used for participant‑level data review, data cleaning, and operational oversight

• Translate study reporting requirements into technical specifications and implement outputs using established frameworks and data standards

• Build and validate data review listings, exception reports, reconciliation outputs between EDC and external data, and operational performance reports

• You communicate clearly with cross‑functional partners to clarify reporting needs and deliver outputs on schedule

• Partner with clinical data management and technology teams to leverage data sources including the Scientific Data Lake, EDC systems, and external data streams

• Monitor routine data refreshes, troubleshoot issues with accuracy, completeness, and integration, and contribute to automation and workflow streamlining

• Keep reporting documentation, specifications, and outputs audit‑ and inspection‑ready in line with GCP, ICH, GDPR, SOPs, and internal quality standards

• You stay curious about reporting tools and methodologies, sharing knowledge of standards and processes to support team learning and continuous improvement

This role requires:

• Bachelor's or Master's degree in Data Science, Computer Science, Life Sciences, or a related field

• 2+ years of experience in clinical data, data visualization, or related disciplines, with a background in building interactive reporting solutions, KPIs, and metrics to support clinical trial oversight

• Proficiency in EDC systems (e.g., Medidata RAVE) and analytics, reporting, and data visualization tools such as SAS, R, Python, JReview, elluminate, Tableau, Power BI, or Spotfire

• Strong understanding of clinical trial processes, clinical data standards (e.g., CDISC), and regulatory requirements (GCP, GDPR, HIPAA)

• Experience with risk‑based data review concepts, data quality standards, and data lifecycle management in a regulated environment

• Experience with data lakes, data pipelines, data integration, automation, and reporting and analytics in a clinical research environment

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, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.