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Elanco

Global animal health pharmaceutical company

Senior Database Programmer

Clinical Research OperationsConfirmed live in the last 24 hours
Full-timeBengaluru, Karnataka, IndiaNo salary listed

About the Job

Requirements

  • A Bachelor of Science degree or equivalent in information technology, statistics, or a scientific field related to animal or human health.
  • At least 10 years of relevant work experience in the animal or human health industry.
  • Demonstrated leadership skills and ability to work within and across interdisciplinary teams.
  • Strong knowledge of GxP, particularly GLP, GCP, and GMP.
  • Good written and verbal communication skills.

Responsibilities

  • Support data management processes and capabilities globally, collaborating with R&D project scientists, global data managers, biostatisticians, and quality assurance to ensure data integrity, quality, validation, and compliance.
  • Search proactively for solutions and work effectively across Elanco R&D teams and external collaborators to achieve R&D deliverables.
  • Create a positive work environment aligned with company objectives and an engaging culture focused on winning.
  • Use methods to deliver individual objectives with high quality, timeliness, and cost-effectiveness, demonstrating adaptability, flexibility, and learning agility.
  • Deploy, validate, test, and implement electronic data capture systems as part of data management strategies.
  • Design, develop, and maintain clinical databases.
  • Maintain case report forms, database objects, forms, edit checks, and procedures.
  • Copy or create study database objects, including DCMs, DCIs, DCI books, forms, edit checks, and procedures, from the global library and customize them to specifications while ensuring database consistency.
  • Perform self-testing of database objects.
  • Copy and customize non-standard objects and programs from the Global Library, as applicable.
  • Build non-standard objects from scratch and ensure they align with specifications, as applicable.
  • Provide user support, troubleshoot, and maintain tools and documentation related to these activities, as needed.
  • Perform annotations, database updates, and quality assurance on case report form annotations for post-production study changes, as applicable.
  • Participate in user acceptance testing when new application releases occur, as applicable.
  • Assemble database components, including forms, folders, matrices, layouts, derivations, validations, edit checks, and custom functions, according to specifications.
  • Migrate databases as needed.
  • Perform quality assurance on the database design document internal audit process in the Electronic Trial Master File tool, as needed.
  • Define scope and conduct impact analysis for migrations and post-production changes, as required.
  • Perform migrations and post-production changes as needed.
  • Generate and provide annotated and non-annotated case report forms, as needed, and configure the coder module as required.
  • Coordinate internal and external resources and capabilities to achieve R&D objectives.
  • Ensure adherence to clinical data collection policies and procedures and maintain industry standards for animal health.
  • Confirm validation and compliance with regulations, including GxP, and guidelines for global data management systems and processes used to collect, manage, report, store, and archive clinical databases.
  • Collaborate with global data management members to develop and review standard operating procedures, quality management system documents, and process documents.
  • Serve as the primary technical expert for complex post-production changes and database migrations, defining scope and conducting impact analysis.
  • Lead development, maintenance, and governance of the Global Library of database objects, driving standardization and efficiency.
  • Coach, mentor, and provide technical guidance to junior database programmers, review their work, and support their professional growth.

Desired Qualifications

  • Vaccine development experience.
  • Working knowledge of electronic systems and their application in animal or human health R&D, maintenance validation, and data pulls.
  • Clinical trial experience, clinical trial data, and study build experience with Rave, Inform, Veeva, Medrio, or another database used to collect clinical trial data.
  • Advanced knowledge of electronic data capture systems.
  • Experience interacting with regulatory authorities and preparing regulatory submissions.
  • Ability to communicate logically and technically, delivering clear, impactful communication tailored to the audience.
  • Organizational planning skills, ability to manage competing priorities, and flexibility to change.
  • Commitment to quality.
  • Ability to work independently or as part of a team.
  • High competency in Microsoft Office.
  • Ability to work additional hours as required and work with staff in irregular time zones.
  • Ability to learn new systems and functions in an evolving technical environment.

About the Company

Elanco

Global animal health pharmaceutical company

Elanco is a global animal health company that develops and sells medicines, vaccines, and preventive care products for livestock and pets. Its portfolio includes prescription medicines, vaccines, parasite controls, and other welfare products used by veterinarians, farmers, and pet owners to prevent or treat disease and improve wellbeing. Since becoming independent after separating from Eli Lilly and acquiring Bayer Animal Health in 2020, it ranks as the world’s second-largest animal health company with a broad, globally distributed product line and direct-to-consumer capabilities. Its goal is to improve animal health and welfare worldwide by providing effective, accessible products and services while growing sustainably.

Company size
5,001-10,000
Company stage
IPO
Headquarters
Indianapolis, IN
Founded
1954

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