# Oracle Programmer I

> Excelya · Bengaluru, India (Hybrid) · Full-time · Posted 2026-06-03

**Workplace:** hybrid

**Department:** Data Management - FSP Non-Competitive

## Description

**About the Job**

Join Excelya, where **Audacity, Care, and Energy** define who we are and how we work. We believe in creating bold solutions and fostering an inclusive environment where collaboration and individual growth go hand in hand.

This role is an exciting opportunity to contribute to a dynamic, ambitious team in Data Management. You will play a critical part in driving innovation and making an impact in the clinical research space, while enjoying a stimulating professional environment that encourages personal and intellectual growth.

_The Oracle Programmer is responsible for providing Oracle Programming input for Data Management activities dedicated to one Sponsor. They are responsible for ensuring all clinical programming aspects per Client’s SOPs are delivered to high quality._  

**Main Responsibilities**

-   _Work closely with the different study stakeholders internally_ 
-   _Responsible for programming using Oracle tools (DMW, LSH)_
-   _Good understanding of SDTM & Data set generations as per the specifications in DMW._
-   _Responsible for setting up for external data vendors integration from specifications in DMW._
-   _Responsible for Transformation mapping as per the specifications._
-   _Responsible for managing external data loading and integrations in DMW._

_Responsible for VC/PD programming in DMW_

## Requirements

**About You**

At Excelya, **taking audacious steps is encouraged**, so we’re looking for individuals who are ready to grow with us and share our values.

• **Experience:**

**2 to 4 years of experience** as an Oracle Programmer or equivalent combination of education, training, and experience 

• **Skills:**

• Good understanding of Oracle DMW tool and study build as per the specifications.

• Experience programming languages, such as PL/SQL, JAVA SCRIPT.

• Knowledge and understanding of ICH GCP and other relevant ICH, EU or FDA guidelines to maintain regulatory compliance. 

• Understanding of Clinical trial process and Data management activities

• Proficient in computer technology used in an office environment (Word, Excel, PowerPoint, MS Project, etc). 

• **Education:**

Bachelor’s degree qualification in a Scientific discipline is preferred. 

• **Languages:**

Fluency in English

## Benefits

**Why Join Us?**

At Excelya, we combine passion for science with enthusiasm for teamwork to redefine excellence in healthcare.

Here’s what makes us unique.

We are a young, ambitious health company representing 900 Excelyates, driven to become Europe’s **leading mid-size CRO** with the **best employee experience**. Our **one-stop provider service model** \- offering full-service, functional service provider, and consulting - enables you to evolve through diverse projects. Working alongside preeminent experts, you will help improve scientific, operational, and human knowledge to enhance the patient's journey.

**Excelling with Care**

At Excelya, **Care** lies at the heart of what we do. We provide equal opportunities for all and foster a diverse, equitable, and inclusive workplace where humility and boldness work hand in hand. Everyone has a space to feel valued, thrive, and collaborate with purpose.

Your challenges become our shared mission. Together, we transform bold ideas into reality, the Excelya way.

**Watch our testimonial video to hear directly from our Excelyates about why Excelya is more than just a workplace—it’s a community built on values.**

**Apply today, become an Excelyate!**

## Apply

[Apply at Excelya](https://apply.workable.com/excelya/j/583D8DEF38/apply)

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