Clinical Research Jobs at Regeneron in Hyderabad
Dreaming about Clinical Research Jobs? Regeneron is offering an exciting opportunity for a Specialist in Clinical Data Reporting based in Hyderabad, India. This pivotal role involves supporting clinical trial oversight and enhancing data review processes. Candidates with a strong background in clinical data management are encouraged to apply for this dynamic position.
About Regeneron
Regeneron is a leading biotechnology company dedicated to inventing, developing, and commercializing medicines that change lives for those with serious diseases. With a strong emphasis on science and innovation, Regeneron is committed to pioneering approaches in research and development. The organization operates globally, with its headquarters in Tarrytown, New York, and a significant presence in Hyderabad, India, focusing on clinical research and data management.
Job Details:
- Job Title: Specialist, Clinical Data Reporting
- Company: Regeneron
- Location: Hyderabad, Telangāna, India (hybrid)
- Job Reference Number: R48587
Job Description
Regeneron is looking for a Specialist in Clinical Data Reporting to join its Data Management team. This position supports clinical trial oversight and study-level data review. The successful candidate will produce accurate reporting outputs that drive data cleaning, medical review, and operational decision-making. Collaborating with clinical data management and cross-functional teams is essential to deliver timely study-level reports.
Key Responsibilities
- Program and maintain standardized clinical data reports and listings for participant-level data review and operational oversight.
- Translate study reporting requirements into technical specifications and implement outputs using established frameworks.
- Build and validate data review listings, exception reports, 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 various data sources.
- Monitor routine data refreshes and troubleshoot issues with accuracy and completeness.
- Maintain reporting documentation in line with GCP, ICH, GDPR, and internal quality standards.
- Share knowledge of reporting tools and methodologies to support team learning and improvement.
Eligibility Criteria
- Bachelor’s or Master’s degree in Life Sciences or a related field.
- 2+ years of experience in clinical data or related disciplines.
- Proficiency in EDC systems and data visualization tools such as SAS, R, or Tableau.
- Strong understanding of clinical trial processes and regulatory requirements.
- Experience with risk-based data review concepts and data quality standards.
- Experience with data lakes and reporting in a clinical research environment.
Why Join Regeneron?
Regeneron offers a unique opportunity to be part of a science-driven organization that is dedicated to making a meaningful difference in the lives of patients. The company fosters an innovative environment where employees can contribute to groundbreaking research and development efforts. Joining Regeneron means being part of a team that values collaboration, integrity, and excellence.
