Manager, Local Lab Delivery
Regeneron · Hyderabad
- Experience7–8 yrs
- SalaryNot disclosed
- Work modeonsite
- Posted29 Sept 2026
About Regeneron
Regeneron is hiring in Hyderabad in pharma biotech. This role looks for around 7+ years of experience.
Skills
- clinical trial processes
- GCP guidelines
- laboratory data management
- clinical operations
- Medidata Rave
- Veeva EDC
- Oracle Inform
- laboratory metadata
- analyte mapping
- test synonym mappings
- local laboratory reference ranges
- unit conversions
- data validation
- Clinical Data Management
- clinical trial operations
The role
A clinical data delivery manager at a pharmaceutical biotechnology company configures clinical trial laboratory data, standardizes laboratory metadata, and validates analyte mappings while coordinating regulated study delivery. Clinical trial processes and GCP guidelines support laboratory data management and quality-controlled clinical operations.
Full job description
Job Summary
The Manager, Local Lab Delivery is responsible for leading a team that supports the setup, management, and delivery of local laboratory data for global clinical trials. This role ensures that laboratory data is accurately configured, standardized, and integrated into clinical study systems while maintaining compliance with regulatory and quality requirements.The individual will work closely with Clinical Data Management, Clinical Operations, Central Laboratories, Local Laboratories, Study Teams, and Technology partners to ensure timely and high-quality laboratory data delivery across multiple studies.
Key ResponsibilitiesLead and manage the Local Lab Delivery team, providing mentorship, coaching, and performance management.Oversee end-to-end local laboratory setup activities for clinical trials.Ensure accurate configuration of:Laboratory metadataAnalyte mappingsTest synonym mappingsLocal laboratory reference rangesUnit conversions and standardizationCollaborate with Clinical Data Management and Clinical Operations teams to support study start-up activities.Review laboratory specifications and ensure alignment with protocol requirements.Drive quality control and data validation processes for laboratory data.Monitor study timelines and ensure deliverables are completed according to project milestones.Identify process improvement opportunities and implement efficiencies within laboratory data workflows.Support inspections, audits, and regulatory compliance activities.Maintain SOPs, work instructions, and operational documentation.Partner with external vendors, CROs, and laboratories to ensure smooth execution of laboratory-related activities.Track team metrics, workload allocation, and resource planning.
Required QualificationsBachelor's degree in Life Sciences, Pharmacy, Biotechnology, Computer Science, or related discipline.7+ years of Clinical Data Management, Laboratory Data Management, or Clinical Trial Operations experience.5+ years of experience supporting local laboratory delivery, laboratory data setup, or laboratory data management in clinical trials.Prior people management or team leadership experience.Strong understanding of clinical trial processes and GCP guidelines.Experience working with EDC systems such as:Medidata RaveVeeva EDCOracle InformOther clinical data platformsExperience managing laboratory reference ranges, analyte mapping, and metadata configuration.