Manager Clinical Data Reporting

Initial Therapeutics, Inc.

India

On-site

INR 1,200,000 - 1,800,000

Full time

14 days+

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Job summary

Initial Therapeutics, Inc. seeks a Manager for Clinical Data Management Reporting to lead the development of clinical data reporting solutions. The role involves transforming complex data into actionable insights and ensures compliance with regulatory standards.

The ideal candidate has 7+ years in clinical data management and proficiency in reporting tools like SAS and Tableau. This office-based position is located in Hyderabad and supports collaboration across various teams.

Qualifications

  • 7+ years of experience in clinical data, reporting, or related domains.
  • Strong hands-on experience in clinical data reporting, analytics, and visualization.
  • Experience working in a regulated clinical or pharmaceutical environment.

Responsibilities

  • Lead the design and maintenance of clinical data reports.
  • Partner with teams to gather and translate reporting requirements.
  • Provide insights for operational performance and decision-making.

Skills

Clinical data management
Data visualization
Problem-solving
Stakeholder management

Education

Bachelors or Masters degree in Data Science, Computer Science, Life Sciences

Tools

Medidata Rave
SAS
Tableau
Power BI

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 a Manager, Clinical Data Management Reporting, you will lead the development and delivery of high-quality clinical data reporting solutions that support efficient data review, operational oversight, and decision-making across clinical development programs. You will play a key role in transforming complex clinical and operational data into clear, actionable insights while ensuring consistency, accuracy, and compliance.

This position is office-based and will be on site at Regenerons Hyderabad office.
A typical day may include the following:
  • Leading the design, development, and maintenance of standardized clinical data reports and listings to support data review and clinical trial oversight
  • Partnering with cross-functional teams to gather reporting requirements and translate them into high-quality, accurate, and timely outputs
  • Delivering participant-level listings, exception reports, and reconciliation outputs to enable efficient data cleaning and review
  • Driving reporting solutions that provide actionable insights for operational performance and decision-making
  • Collaborating with data management and technology teams to leverage EDC systems, data lakes, and external data sources
  • Providing subject matter expertise in clinical data reporting, data structures, and reporting workflows
  • Identifying opportunities for automation and process improvement to enhance reporting efficiency and scalability
  • Monitoring data flows and troubleshooting issues related to data accuracy, completeness, and refresh cycles
  • Supporting inspection readiness by ensuring reporting outputs are compliant, traceable, and audit-ready
  • Delivering insights to identify risks, bottlenecks, and opportunities for operational improvement
  • Ensuring compliance with regulatory requirements such as GCP, ICH, and data privacy standards
  • Supporting training initiatives and development of reporting frameworks, standards, and documentation
  • Providing guidance and mentorship to team members and contributing to team development
This job may be for you if you have:
  • Strong experience in clinical data management, reporting, and data visualization
  • Good understanding of clinical trial processes, data standards (CDISC), and regulatory requirements
  • Experience working with EDC systems such as Medidata Rave
  • Proficiency in reporting and visualization tools such as SAS, R, Tableau, Power BI, Spotfire, or similar
  • Experience with data integration, data lakes, data pipelines, and automation frameworks
  • Strong knowledge of data lifecycle management and risk-based data review concepts
  • Excellent problem-solving, communication, and stakeholder management skills
To be considered for this role, you must have:
  • Bachelors or Masters degree in Data Science, Computer Science, Life Sciences, or a related field
  • 7+ years of experience in clinical data, reporting, or related domains
  • Strong hands‑on experience in clinical data reporting, analytics, and visualization
  • Experience working in a regulated clinical or pharmaceutical 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, 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.

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