Associate Director Clinical Data Reporting

Regeneron Pharmaceuticals, Inc; Hyderabad; On-site; INR 2,500,000 - 3,500,000; Full time

Benefits offered by this job

Health and wellness programs

401(k) company match

Annual bonuses

Paid time off

Job summary

Regeneron Pharmaceuticals, Inc. is seeking an Associate Director for Clinical Data Reporting in Hyderabad. This role involves leading oversight for clinical data reporting and ensuring high-quality outputs across development programs.

The ideal candidate will possess extensive experience in clinical data management and leadership skills, with a strong focus on adhering to regulatory standards. This position fosters an inclusive culture offering comprehensive benefits depending on locality.

Qualifications

• 10+ years of experience in clinical data management or related areas within pharma/biotech.
• At least 5+ years of leadership experience managing teams and mentoring staff.
• Strong experience in clinical data reporting, programming, and analytics.

Responsibilities

• Leading program‑level oversight for clinical data reporting.
• Driving development of participant‑level listings and exception reports.
• Collaborating with cross‑functional teams to align priorities.
• Ensuring adherence to regulatory requirements and quality standards.

Skills

Clinical data management

Data visualization

Problem-solving

Analytical skills

Education

Bachelor's degree

Tools

SAS

R

Tableau

Power BI

Spotfire

Job description

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 an Associate Director, Clinical Data Reporting, you will provide leadership and operational oversight for clinical and external data reporting across clinical development programs. You will drive the delivery of high‑quality data programming outputs, reconciliation workflows, and reporting solutions that support clinical trial quality, compliance, and informed decision‑making.

This position is office‑based and will be on site at Regeneron’s Hyderabad office.

A typical day may include the following:

• Leading program‑level oversight for clinical data reporting and programming deliverables across development programs
• Driving development of participant‑level listings, exception reports, external data reconciliation outputs, and operational metrics
• Establishing and maintaining reporting standards, templates, and scalable programming approaches
• Providing subject matter expertise in data programming, transformation, and visualization to enhance reporting capabilities
• Collaborating with cross‑functional teams to align priorities and ensure timely delivery of reporting outputs
• Ensuring adherence to regulatory requirements, quality standards, and inspection readiness expectations
• Driving continuous improvement and automation of reporting workflows
• Identifying and managing risks related to data quality and delivery timelines
• Monitoring KPIs to assess reporting performance and enhance processes
• Leading and mentoring reporting and programming teams to drive operational excellence

This job may be for you if you have:

• Strong expertise in clinical data management, reporting, and data visualization
• Experience working with clinical trial data, including eCRF and external data sources such as PK, biomarker, imaging, and ECG
• Deep understanding of data transformation, validation, and reconciliation processes
• Strong knowledge of regulatory standards such as ICH‑GCP, CDISC, and 21 CFR Part 11
• Experience with tools such as SAS, R, Tableau, Power BI, Spotfire, or similar reporting platforms
• Proven ability to work cross‑functionally and manage stakeholder expectations
• Strong analytical, problem‑solving, and communication skills

To be considered for this role, you must have:

• Bachelor’s degree with 10+ years of relevant experience
• 10+ years of experience in clinical data management or related areas within pharma/biotech
• At least 5+ years of leadership experience managing teams and mentoring staff
• Strong experience in clinical data reporting, programming, and analytics

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.

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.