Senior Clinical Data Coordinator Openings at ICON plc

ICON Hiring Clinical Data Coordinator II – Clinical Data Management Opportunity in Bangalore

ICON plc is currently recruiting for the role of Clinical Data Coordinator II within the Clinical Data Management division. The position is based in Bangalore, India, with flexible options to work remotely or from the office. This opportunity is suitable for life sciences graduates who have experience in clinical data management and want to work in global clinical trials supporting pharmaceutical and biotechnology research programs.

The Clinical Data Coordinator II role focuses on maintaining electronic clinical trial data systems, ensuring accurate data collection from research sites, supporting clinical data review processes, and collaborating with cross‑functional clinical teams. Professionals in this role contribute directly to the integrity of clinical trial data that supports regulatory submissions and the development of innovative therapies.

Candidates with a background in life sciences, clinical research, or healthcare analytics who have knowledge of clinical trial databases and regulatory guidelines will find this role highly aligned with career growth in clinical data management and pharmaceutical research operations.

Company Overview

ICON plc is a world‑leading healthcare intelligence and clinical research organization that partners with pharmaceutical, biotechnology, and medical device companies to accelerate drug development. With operations across multiple countries, ICON supports sponsors through every phase of clinical development, including study design, data management, regulatory consulting, and real‑world evidence generation.

The company combines advanced clinical research technology with scientific expertise to support the development of innovative treatments that improve patient outcomes worldwide. ICON is known for its strong commitment to quality, innovation, and data‑driven clinical research.

Employees at ICON work in a collaborative environment that values diversity, continuous learning, and professional development. By joining the organization, professionals gain exposure to global clinical trials, regulatory compliance standards, and advanced clinical data management systems used across the pharmaceutical industry.

Job Role and Responsibilities

The Clinical Data Coordinator II will support clinical data management activities for ongoing clinical studies. The role involves maintaining study databases, performing data reconciliation, and ensuring clinical trial data is accurate, complete, and compliant with regulatory requirements.

Key responsibilities include:

• Assisting the Data Management Study Lead in maintaining electronic Case Report Forms (eCRF)
• Supporting development and updates of Data Validation Specifications and study procedures
• Managing reconciliation of clinical trial data and third‑party datasets based on predefined data review plans
• Tracking study metrics and communicating project progress with clinical data scientists and project teams
• Identifying and resolving clinical data discrepancies through systematic data review
• Responding to data related queries from project teams and recommending solutions
• Supporting maintenance of study documentation and data management records
• Ensuring clinical trial datasets comply with regulatory standards and quality guidelines
• Collaborating with cross‑functional teams involved in clinical research projects

The role plays a critical part in ensuring that clinical trial data is reliable, traceable, and ready for regulatory submission during pharmaceutical drug development.

Eligibility and Qualifications

Candidates applying for this clinical data management role should meet the following requirements.

Required Education

Bachelor’s degree in a relevant discipline related to healthcare or life sciences.

Relevant courses include:

Pharmacy, Biotechnology, Biochemistry, Microbiology, Life Sciences, Biomedical Sciences, Clinical Research, Pharmacology, Public Health, Molecular Biology

Experience

Experience in clinical data management within the pharmaceutical, biotechnology, or CRO industry is preferred.

Candidates should have familiarity with clinical trial databases and electronic data capture systems.

Required Skills

• Knowledge of clinical data management processes in clinical trials
• Experience working with electronic data capture systems such as Medidata or Oracle RDC
• Strong analytical thinking and data review capability
• Attention to detail and ability to work in fast‑paced clinical research environments
• Excellent written and verbal communication skills
• Ability to collaborate with cross‑functional clinical research teams

Preferred Knowledge

• Understanding of regulatory guidelines including ICH‑GCP standards
• Experience with clinical trial database validation and reconciliation processes

Location and Salary

Job Location: Bangalore, India

Work Model: Remote or Office (Hybrid flexibility depending on project requirements)

Application Process

Candidates interested in this clinical data management opportunity can apply through the official ICON careers portal.

Apply here:

https://careers.iconplc.com/job/clinical-data-coordinator-ii-in-india-bangalore-jid-47885

Applicants are encouraged to submit applications through the official website to ensure authenticity and avoid recruitment scams.

Frequently Asked Questions

What does a Clinical Data Coordinator do?

A Clinical Data Coordinator manages and reviews clinical trial data to ensure accuracy, completeness, and compliance with regulatory standards before it is used in analysis and regulatory submissions.

What qualifications are required for this role?

Candidates should have a bachelor’s degree in life sciences such as Pharmacy, Biotechnology, Microbiology, or Clinical Research.

What systems should candidates be familiar with?

Experience with electronic data capture platforms like Medidata or Oracle RDC is beneficial for this role.

Is clinical research experience required?

Yes, candidates should have some experience or knowledge of clinical data management processes in the pharmaceutical or biotechnology industry.

How can I apply for this job?

Candidates can apply through the official ICON careers website using the application link provided above.

Job Summary

Company	ICON plc
Vacancies	Clinical Data Coordinator II
Required Education	Pharmacy, Biotechnology, Biochemistry, Microbiology, Life Sciences, Biomedical Sciences, Clinical Research, Pharmacology, Public Health, Molecular Biology
Experience	Clinical data management experience in pharma, biotech, or CRO industry

Tagged as: Pharma Jobs in Bangalore