Specialist, Clinical Data Reporting

Regeneron; Hyderabad; Hybrid; INR 600,000 - 900,000; Full time

Job summary

Regeneron is looking for a Specialist in Clinical Data Reporting to join their Data Management team in Hyderabad, India. This hybrid role focuses on producing accurate reports that assist clinical trial oversight and data review, while collaborating with cross-functional teams.

The ideal candidate should have a degree in a relevant field and over 2 years of experience in clinical data, with proficiency in various EDC systems and data visualization tools. Join our diverse and inclusive team!

Qualifications

• 2+ years of experience in clinical data or related disciplines.
• Strong understanding of clinical trial processes and data standards.
• Experience with risk-based data review and data lifecycle management.

Responsibilities

• Produce standardized clinical data reports and listings.
• Translate study reporting requirements into technical specifications.
• Monitor data refreshes and contribute to automation.

Skills

Experience in clinical data

Data visualization proficiency

Proficiency in EDC systems

Analysis with SAS, R, Python

Education

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

Tools

Medidata RAVE

Tableau

Power BI

Job description

Job Summary

Regeneron is 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. The position involves producing 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.

Location and Work Arrangement

Hyderabad, India – Hybrid work model.

Key Responsibilities

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

Qualifications

• 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, illuminate, 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.

Equal Opportunity Employer

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.