ICON plc is hiring for Intern, Clinical Data Science Programmer, Statistical Programmer II, Site Specialist II & eCOA Review Associate

Published on

November 20, 2025

Intern, Clinical Data Science Programmer, Statistical Programmer II, Site Specialist II & eCOA Review Associate

ICON plc

B.Pharm, M.Pharm, Pharm.D, Msc, BSc, Lifesciences, Business, Stats, Maths, CS

Bangalore, Chennai, and Trivandrum

0 - 4 Years+

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ICON plc, a global leader in clinical research and healthcare intelligence, has announced five major job openings in India across Bangalore, Chennai, and Trivandrum. These roles span clinical programming, site activation, eCOA review, and internships, offering excellent opportunities for candidates in life sciences, pharmacy, statistics, computer science, and clinical operations.

If you are looking to start or advance your career in the clinical research industry, ICON’s latest recruitment drive provides high-growth, high-impact roles backed by world-class training, competitive pay, and a strong culture of inclusion.

This article covers all five roles in one place—responsibilities, qualifications, salary, benefits, and how to apply—optimized for Google Search, Discover, and AI Overviews.

1. Intern — ICON plc, Bangalore (Office Non-Flex)

Responsibilities

Assist with data collection, research, and analysis.
Support team meetings with documentation and idea contributions.
Prepare reports, presentations, and internal materials.
Perform administrative and day-to-day coordination tasks.
Participate in professional development and internal networking.

Qualifications

Pursuing a Bachelor’s or Master’s degree (Life Sciences, Business, Communications, Pharma, etc.).
Strong communication and organizational skills.
Ability to multitask and learn quickly.
Proficiency in MS Office; analytical tools are a plus.

Salary (Option B Range)

₹25,000 – ₹40,000 per month

2. Clinical Data Science Programmer — Bangalore, Chennai, Trivandrum

Responsibilities

Develop and validate SAS/R/Python code for clinical trial datasets.
Collaborate with data scientists and statisticians on analytical needs.
Ensure code quality and compliance with FDA/ICH/GCP guidelines.
Maintain programming documentation and specifications.
Review analysis datasets, TLFs, and study outputs.

Qualifications

Degree in Computer Science, Statistics, Life Sciences, or related fields.
Programming experience using SAS / R / Python / Medidata Rave.
Understanding of statistical methods and clinical data workflows.
Strong attention to detail and team communication.

Salary

₹8 – ₹14 LPA

3. Site Specialist II — Bangalore / Chennai (Office with Flex)

Responsibilities

Manage site activation tasks (essential documents, green-light readiness).
Handle ICF customization, translation processes, and IRB/EC submissions.
Oversee contract workflows, amendments, and negotiations.
Document all activities in eTMF systems.
Coordinate with cross-functional global teams.

Qualifications

Bachelor’s degree in Life Sciences or Business.
3+ years experience in site start-up, EC submissions, or contract management.
Knowledge of ICF workflows and regulatory documentation.
Ability to manage multiple priorities and global shifts.

Salary

₹9 – ₹14 LPA

4. eCOA Screen Review Associate — India / Poland / Bulgaria

Responsibilities

Review eCOA screenshots to ensure compliance with best practices.
Conduct functional testing across multiple device platforms.
Work with clients to resolve issues and validate usability.
Handle multiple global projects simultaneously.
Generate analytical reports and perform QC tasks.

Qualifications

Bachelor’s degree in Life Sciences, Healthcare, or Business.
2 years’ experience in clinical coordination, client service, or project management (preferred).
Strong communication, English proficiency, and attention to detail.
Familiarity with COA/PRO tools is a bonus.