ICON plc is hiring Clinical Data Coordinator II (CDC II) professionals with 3–5 years of experience in Clinical Data Management (CDM) for its teams in Chennai and Thiruvananthapuram. This opportunity is ideal for candidates with experience in clinical data management systems, Electronic Data Capture (EDC) platforms, clinical trial processes, and risk-based monitoring principles.

With increasing demand for skilled professionals in the clinical research industry, Clinical Data Management jobs at ICON provide an excellent opportunity for experienced CDM professionals to grow their careers with a global pharmaceutical and life sciences organization.

Job Overview – ICON Clinical Data Coordinator II

About ICON plc

ICON plc is a global clinical research organization (CRO) supporting pharmaceutical, biotechnology, and healthcare companies in conducting clinical trials worldwide. The company provides services across clinical development, data management, pharmacovigilance, regulatory affairs, and technology-enabled clinical research solutions.

Key Responsibilities – Clinical Data Coordinator II

The selected candidate will support clinical data management activities and ensure high-quality clinical trial data throughout the drug development lifecycle.

Responsibilities include:

• Manage and review clinical trial data according to study protocols and data management plans.
• Work with Clinical Data Management Systems (CDMS) and Electronic Data Capture (EDC) platforms.
• Perform data review activities to identify discrepancies and improve data quality.
• Support risk-based monitoring approaches during clinical studies.
• Coordinate with cross-functional clinical research teams including Clinical Operations, Data Managers, and Clinical Trial teams.
• Apply knowledge of clinical study phases and drug development processes.
• Support database cleaning, query management, and data validation activities.
• Ensure compliance with clinical research standards, SOPs, and regulatory requirements.

Required Qualifications and Skills

Candidates applying for the ICON Clinical Data Coordinator II position should have:

Educational Qualification

• Bachelor’s degree in Life Sciences, Pharmacy, Biotechnology, Medicine, or related healthcare fields.
• Equivalent clinical research or healthcare qualifications may also be considered.

Experience Requirements

• 3–5 years of experience in Clinical Data Management.
• Experience working with clinical data management systems.
• Hands-on knowledge of Electronic Data Capture (EDC) software.
• Understanding of clinical trial phases and drug development processes.
• Knowledge of risk-based monitoring principles.

Key Skills:

• Clinical Data Management (CDM)
• Electronic Data Capture (EDC)
• Clinical Trial Data Review
• Database Cleaning
• Query Management
• Clinical Research Processes
• Risk-Based Monitoring (RBM)
• Drug Development Lifecycle

Why Apply for ICON Clinical Data Management Jobs?

Working as a Clinical Data Coordinator II at ICON offers professionals the opportunity to:

✅ Work with a leading global Clinical Research Organization
✅ Gain exposure to international clinical trials
✅ Develop expertise in CDM systems and EDC technologies
✅ Collaborate with global clinical research teams
✅ Build a long-term career in clinical research and life sciences

ICON Clinical Data Coordinator II Salary in India

The estimated salary range for a Clinical Data Coordinator II with 3–5 years of experience in India is approximately:

₹5 LPA – ₹9 LPA

Salary may vary depending on experience, technical skills, location, and previous clinical data management expertise.

Who Can Apply?

This opportunity is suitable for:

• Clinical Data Coordinators
• Clinical Data Management Associates
• Clinical Research Professionals
• CDM Specialists
• Healthcare and Life Sciences professionals looking for CRO career opportunities

ICON also encourages applications from women returning to work and differently-abled candidates.

How to Apply

Application Link