Elluminate Programmer New

NetVerks Inc.; Chennai; Híbrido; INR 900.000 - 1.500.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Health and wellbeing programmes

Retirement and pension plans

Life assurance and disability coverage

Learning and development opportunities

Employee assistance programmes

Descripción de la vacante

ICON Strategic Solutions is seeking an experienced Lead Clinical Data Science Programmer (Elluminate) to design and develop data solutions for clean, analyze and report complex clinical trial data. The role is based in Bangalore/Chennai within sponsor-dedicated model teams.

You will create reusable checks, collaborate on cross-functional rules, and ensure adherence to SOPs while advancing reporting capabilities and data management standards.

Formación

• Bachelor's degree or equivalent in CS, stats, biostatistics, mathematics, biology or health-related field.
• Knowledge of drug development process and regulatory data standards; CDISC/SDTM preferred.
• 3–5 years’ experience in programming listings and/or visualizations with Elluminate, JReview or Veeva.
• Hands-on experience with Elluminate report development and data cleaning.
• Proficiency in SQL, SAS, R or Python.
• Familiarity with clinical db systems and MS Office tools.

Responsabilidades

• Create data cleaning reporting solutions and study status visualizations with governance.
• Document reports and assets across study lifecycles.
• Develop reusable checks with data engineers and config specialists.
• Collaborate on business rules and automated check libraries across TAU.
• Provide data analytics support for data validation and cleaning.
• Enhance reporting tools and libraries for clinical trial data review.

Conocimientos

SQL

Python

R

SAS

CQL

Regulatory knowledge

Educación

Bachelor's degree in computer science or related field

Herramientas

Elluminate

JReview

Veeva CDB

Metadata Rave

Inform

Descripción del empleo

Elluminate Programmer, Bangalore/Chennai

Elluminate Programmer, Bangalore/ChennaiAt ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise. As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide. As a Lead Clinical Data Science Programmer (Elluminate) at ICON, you will design and develop clinical data solutions, ensuring the efficient handling, analysis, and reporting of complex clinical trial data.

What You Will Do

• Create data cleaning reporting solutions with appropriate oversight that support the quality and timely delivery of data cleaning, study status metric, and monitoring reports and visualizations required per standard and study specific data review plans.
• Create any documentation needed for reports throughout the lifespan of the study and/or asset for all deliverables.
• Develop a library of reusable checks working closely with data engineers and config specialists.
• Collaborate with cross functional teams in creating business rules and automated check library across TAU.
• Complies with applicable SOPs and work practices.
• Serves as a technical resource for creating data analytics to help with data validation and cleaning.
• Supports knowledge development of others on reporting tools that support the accuracy and integrity of study data.
• Provide programming expertise for data cleaning to efficiently ensure high quality data.
• Enhances available reporting tools/macros/libraries or creates new ones to support the review of clinical trial data and trial status information for cross‑functional use and provides input on data management reporting standards as required.
• Creates and tests listings for data review.
• Ensure operational excellence in collaboration with partners and colleagues for application of standards and develop data cleaning reports in support of the data review plan, in collaboration with the Clinical Data Management and medical reviewers.
• Develop innovative, advanced new concepts that improve processes.

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.

Education & Competencies (Technical and Behavioral)

• Bachelor's degree in computer science, statistics, biostatistics, mathematics, biology or other health related field or equivalent experience that provides the skills and knowledge necessary to perform the job.
• Knowledge of drug development process.
• Understanding regulatory requirements and relevant data standards; CDISC and SDTM knowledge and experience are preferable.
• Minimum 3-5 years’ experience in programming listings and/or visualizations with any of the following Veeva CDB, JReview and Elluminate.
• Hands‑on experience with report development in Elluminate.
• Experience with one of these languages: CQL, SQL, SAS, R, Python.
• Knowledge of clinical database systems (Metadata Rave, Veeva, Inform).
• Proficiency in the use of Microsoft Office Suite of tools (Outlook, Word, Excel, etc.).
• Strong working knowledge of clinical trial terminology.
• Must be able to work in a fast‑paced environment.
• Ability to work independently, take initiative and complete tasks to deadlines.

Rewards & Benefits

• Competitive base salary and performance related incentives.
• Health and wellbeing programmes including medical, dental, and vision coverage where applicable.
• Retirement and pension plans.
• Life assurance and disability coverage.
• Employee assistance programmes and wellbeing resources.
• Learning and development opportunities through structured training and career pathways.

Benefits may vary depending on role and location.

Visit our careers site to read more about the benefits ICON offers.

Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.

If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.