Specialist Local Lab Delivery

Regeneron Pharmaceuticals; Hyderabad; On-site; INR 1,200,000 - 2,400,000; Full time

Job summary

Regeneron Pharmaceuticals seeks a Specialist in Local Lab Delivery to ensure laboratory data used in clinical studies is accurate and ready when teams need it. You will collaborate with Clinical Data Management, Clinical Operations, study teams, and external providers to manage local laboratory reference ranges and metadata throughout the study lifecycle.

This on-site Hyderabad role focuses on maintaining lab data and metadata, updating information to support start-up, delivery, and database

Qualifications

• Bachelor's degree required with data management relevance.
• 2+ years in Clinical Data Management or lab data delivery.
• Experience with local laboratory reference ranges and metadata.

Responsibilities

• Review and track local laboratory reference range documents for completeness and currency.
• Maintain accurate laboratory data and metadata including tests, units, synonyms, and details.
• Configure and update local laboratory information to support start-up, delivery, and database lock.
• Investigate data discrepancies and escalate risks as needed.
• Collaborate with study teams and external providers to deliver activities on time.
• Maintain inspection-ready documentation and audit trails.
• Drive process improvements through automation and metadata standardization.

Skills

Analytical

Organizational skills

Communication

Cross-functional collaboration

Lab data systems

Validation testing

Metadata standardization

Automation

AI workflows

Clinical Data Management experience

Laboratory reference ranges

GxP knowledge

Education

Bachelor's degree in science, health, data management, mathematics, computing, or a related field

Tools

Lab data systems

Job description

Build our future together:

At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. As a Specialist in Local Lab Delivery, you will help ensure laboratory data used in clinical studies is accurate, consistent, and ready when study teams need it. You will partner with Clinical Data Management, Clinical Operations, study teams, and external providers to manage local laboratory reference ranges and supporting metadata throughout the study lifecycle. Your work will strengthen data quality, support timely study delivery and database lock, and help advance more standardized, efficient, and technology-enabled ways of working across our growing global organization.

When & where:

Location: Hyderabad

Discover your role:

• Review and track local laboratory reference range documents to ensure they are complete, current, and available for study activities.
• Maintain accurate laboratory data and metadata, including tests, reference ranges, units, conversion factors, synonyms, and laboratory details.
• Configure and update local laboratory information to support study start-up, ongoing delivery, and database lock.
• Investigate and resolve laboratory data discrepancies, escalating risks and quality concerns when appropriate.
• Partner with Clinical Data Management, Clinical Operations, study teams, and external providers to deliver activities on time.
• Assess and implement updates when laboratories, reference ranges, or supporting information change during a study.
• Maintain clear, inspection-ready documentation and audit trails in line with quality and regulatory expectations.
• Improve processes through metadata standardization, automation, and technology-enabled ways of working.

This role requires:

• A bachelor's degree in science, health, data management, mathematics, computing, or a related field.
• At least 2 years of Clinical Data Management experience, including hands‑on experience supporting local laboratory delivery in biotechnology, pharmaceuticals, a CRO, or healthcare.
• Experience managing local laboratory reference ranges and metadata, including analytes, units, conversion factors, test synonyms, and laboratory documentation.
• Ability to review source documents, identify data quality issues, investigate discrepancies, and deliver accurate work within study timelines.
• Knowledge of clinical trial processes, data quality expectations, GxP requirements, and inspection readiness.
• Strong analytical, organizational, communication, and cross‑functional collaboration skills.
• Experience with laboratory administration or clinical data systems and the validation or testing of related technologies.
• Experience contributing to metadata standardization, process improvement, automation, or AI‑enabled workflows.

Does this sound like you? We are committed to building a workplace with an inclusive culture. 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, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.

Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/ . For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter.

Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.

As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.

For jobs in Canada: this posting is for an existing position.