Career as Senior Manager Clinical Sciences at Regeneron

Regeneron pushes the boundaries of scientific discovery and accelerates drug development using our proprietary technologies, such as VelociSuite®, which produces optimized fully human antibodies and new classes of bispecific antibodies. We are shaping the next frontier of medicine with data-powered insights from the Regeneron Genetics Center® (RGC) and pioneering genetic medicine platforms, enabling us to identify innovative targets and complementary approaches to potentially treat or cure diseases.

Post : Senior Manager Clinical Sciences

Job Description
• Lead the day-to-day functional management of a centralized pool of Clinical Data Reviewers and Medical Narrative Reviewers, serving as the primary point of contact for resource coordination across studies and programs.
• Translate portfolio-level study assignments into resource prioritization plans and monitor delivery against achievements and key operational objectives.
• Personally perform clinical data review, query management, and medical narrative review activities when required to support coverage gaps, onboarding periods, workload surges, or quality remediation initiatives.
• Establish, monitor, and report key performance indicators (KPIs), ensuring compliance with SOPs, Restricted Data Handling requirements, and quality standards.
• Lead onboarding and training activities, including SOP assignment, systems access support, and reviewer readiness assessments in partnership with Clinical Scientists and Study Medical Directors.
• Drive capacity forecasting and workforce planning activities by collaborating with Clinical Scientist Leads and Clinical Program Leads to align resources with study timelines and business needs.
• Ensure continuity of governance and operational excellence during team transitions, turnover, protocol changes, and study closeouts.
• Support knowledge management, institutional learning, and consistency of reviewer practices across the portfolio.
• Represent the Clinical Sciences function within the GCC and contribute to strategic initiatives focused on quality, efficiency, and process improvement.

Candidate Profile
• Advanced degree in a scientific or medical field; MD, PhD, PharmD, or equivalent strongly preferred.
• Minimum 7 years of experience in clinical research, drug development, pharmaceutical operations, or related healthcare industry environments.
• Hands-on experience performing clinical data review and/or medical review of patient narratives.
• Practitioner-level knowledge of EDC systems, clinical data review tools, query management processes, and narrative review activities.
• Demonstrated experience managing, coaching, and developing clinical and medical professionals within a matrixed and cross-functional environment.
• Strong operational leadership, quality governance, and stakeholder management capabilities.
• Excellent communication, collaboration, and interpersonal skills with the ability to influence and lead distributed teams.
• Strong analytical, critical thinking, and problem-solving abilities.
• Scientific and medical competence to understand, evaluate, and communicate complex clinical development concepts.
• Willingness to perform hands-on review activities as needed to ensure quality, continuity, and timely delivery.
• High level of integrity, professionalism, and discretion when handling sensitive information.

Additional Information
Experience : Minimum 7 years
Qualification : PhD, PharmD, or equivalent strongly preferred
Location : Hyderabad, Telangana, India
Industry Type : Pharma/ Healthcare/ Clinical research
Functional Area : Global Development
End Date : 20th September 2026